Linked Data
ClinVar Variation Id:
163139
ClinVar RCV Id:
RCV000556876
dbSNP Id:
rs727502973
ExAC:
5:13788830 G / C
gnomAD v2:
5-13788830-G-C
gnomAD v3:
5-13788721-G-C
gnomAD v4:
5-13788721-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13788721G>C , CM000667.2:g.13788721G>C | GRCh38 |
| NC_000005.9:g.13788830G>C , CM000667.1:g.13788830G>C | GRCh37 |
| NC_000005.8:g.13841830G>C | NCBI36 |
| NG_013081.1:g.160760C>G | |
| NG_013081.2:g.160760C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.8642C>G MANE Select | ENSP00000265104.4:p.Ala2881Gly | |
| ENST00000681290.1:c.8597C>G | ENSP00000505288.1:p.Ala2866Gly | |
| ENST00000265104.4:c.8642C>G | ENSP00000265104.4:p.Ala2881Gly | |
| NM_001369.2:c.8642C>G | NP_001360.1:p.Ala2881Gly | |
| XM_005248262.2:c.8597C>G | XP_005248319.1:p.Ala2866Gly | |
| XM_011513990.1:c.8642C>G | XP_011512292.1:p.Ala2881Gly | |
| XR_925598.1:n.8849C>G | ||
| XM_005248262.3:c.8750C>G | XP_005248319.2:p.Ala2917Gly | |
| XM_017009177.1:c.8750C>G | XP_016864666.1:p.Ala2917Gly | |
| XM_017009178.1:c.7655C>G | XP_016864667.1:p.Ala2552Gly | |
| XM_017009179.2:c.7655C>G | XP_016864668.1:p.Ala2552Gly | |
| XM_017009180.1:c.8750C>G | XP_016864669.1:p.Ala2917Gly | |
| XM_017009181.1:c.8750C>G | XP_016864670.1:p.Ala2917Gly | |
| XM_017009182.1:c.8750C>G | XP_016864671.1:p.Ala2917Gly | |
| XM_017009183.1:c.8750C>G | XP_016864672.1:p.Ala2917Gly | |
| XM_017009184.1:c.8750C>G | XP_016864673.1:p.Ala2917Gly | |
| XM_017009185.1:c.3839C>G | XP_016864674.1:p.Ala1280Gly | |
| XM_017009186.1:c.3392C>G | XP_016864675.1:p.Ala1131Gly | |
| XM_017009188.1:c.2729C>G | XP_016864677.1:p.Ala910Gly | |
| XM_024454388.1:c.7655C>G | XP_024310156.1:p.Ala2552Gly | |
| XM_024454389.1:c.7244C>G | XP_024310157.1:p.Ala2415Gly | |
| XR_001742034.1:n.8767C>G | ||
| XR_001742035.1:n.8767C>G | ||
| NM_001369.3:c.8642C>G MANE Select | NP_001360.1:p.Ala2881Gly |