Linked Data
ClinVar Variation Id:
236647
ClinVar RCV Id:
RCV000229496
RCV000562662
RCV000677749
RCV001156936
RCV001193538
RCV003316239
RCV003477779
dbSNP Id:
rs772806807
ExAC:
5:112137003 G / A
gnomAD v2:
5-112137003-G-A
gnomAD v3:
5-112801306-G-A
gnomAD v4:
5-112801306-G-A
COSMIC:
COSM327129
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112801306G>A , CM000667.2:g.112801306G>A | GRCh38 |
| NC_000005.9:g.112137003G>A , CM000667.1:g.112137003G>A | GRCh37 |
| NC_000005.8:g.112164902G>A | NCBI36 |
| NG_008481.4:g.113786G>A , LRG_130:g.113786G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.757G>A | ENSP00000484935.2:p.Gly253Ser | |
| ENST00000504915.3:c.757G>A | ENSP00000473355.2:p.Gly253Ser | |
| ENST00000505084.2:n.813G>A | ||
| ENST00000505350.2:c.*763G>A | ENSP00000481752.1:n.*763G>A | |
| ENST00000507379.6:c.703G>A | ENSP00000423224.2:p.Gly235Ser | |
| ENST00000509732.6:c.757G>A | ENSP00000426541.2:p.Gly253Ser | |
| ENST00000512211.7:c.757G>A | ENSP00000423828.3:p.Gly253Ser | |
| ENST00000257430.9:c.757G>A MANE Select | ENSP00000257430.4:p.Gly253Ser | |
| ENST00000257430.8:c.757G>A | ENSP00000257430.4:p.Gly253Ser | |
| ENST00000507379.5:c.703G>A | ENSP00000423224.1:p.Gly235Ser | |
| ENST00000508376.6:c.757G>A | ENSP00000427089.2:p.Gly253Ser | |
| ENST00000508624.5:c.757G>A | ENSP00000424265.1:p.Gly253Ser | |
| ENST00000512211.6:c.757G>A | ENSP00000423828.2:p.Gly253Ser | |
| NM_000038.5:c.757G>A | NP_000029.2:p.Gly253Ser | |
| NM_001127510.2:c.757G>A | NP_001120982.1:p.Gly253Ser | |
| NM_001127511.2:c.703G>A | NP_001120983.2:p.Gly235Ser | |
| NM_001354895.1:c.757G>A | NP_001341824.1:p.Gly253Ser | |
| NM_001354896.1:c.757G>A | NP_001341825.1:p.Gly253Ser | |
| NM_001354897.1:c.787G>A | NP_001341826.1:p.Gly263Ser | |
| NM_001354898.1:c.682G>A | NP_001341827.1:p.Gly228Ser | |
| NM_001354899.1:c.673G>A | NP_001341828.1:p.Gly225Ser | |
| NM_001354900.1:c.580G>A | NP_001341829.1:p.Gly194Ser | |
| NM_001354901.1:c.580G>A | NP_001341830.1:p.Gly194Ser | |
| NM_001354902.1:c.787G>A | NP_001341831.1:p.Gly263Ser | |
| NM_001354903.1:c.757G>A | NP_001341832.1:p.Gly253Ser | |
| NM_001354904.1:c.682G>A | NP_001341833.1:p.Gly228Ser | |
| NM_001354905.1:c.580G>A | NP_001341834.1:p.Gly194Ser | |
| NM_001354906.1:c.-279G>A | NP_001341835.1:n.-279G>A | |
| NM_000038.6:c.757G>A MANE Select | NP_000029.2:p.Gly253Ser | |
| NM_001127510.3:c.757G>A | NP_001120982.1:p.Gly253Ser | |
| NM_001127511.3:c.703G>A | NP_001120983.2:p.Gly235Ser | |
| NM_001354895.2:c.757G>A | NP_001341824.1:p.Gly253Ser | |
| NM_001354896.2:c.757G>A | NP_001341825.1:p.Gly253Ser | |
| NM_001354897.2:c.787G>A | NP_001341826.1:p.Gly263Ser | |
| NM_001354898.2:c.682G>A | NP_001341827.1:p.Gly228Ser | |
| NM_001354899.2:c.673G>A | NP_001341828.1:p.Gly225Ser | |
| NM_001354900.2:c.580G>A | NP_001341829.1:p.Gly194Ser | |
| NM_001354901.2:c.580G>A | NP_001341830.1:p.Gly194Ser | |
| NM_001354902.2:c.787G>A | NP_001341831.1:p.Gly263Ser | |
| NM_001354903.2:c.757G>A | NP_001341832.1:p.Gly253Ser | |
| NM_001354904.2:c.682G>A | NP_001341833.1:p.Gly228Ser | |
| NM_001354905.2:c.580G>A | NP_001341834.1:p.Gly194Ser | |
| NM_001354906.2:c.-279G>A | NP_001341835.1:n.-279G>A |