Linked Data
ClinVar Variation Id:
307144
ClinVar RCV Id:
RCV000263321
RCV000294966
RCV000315912
RCV000321831
RCV000372893
RCV000374276
RCV002411200
dbSNP Id:
rs886048941
gnomAD v2:
12-110252431-A-G
gnomAD v4:
12-109814626-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.109814626A>G , CM000674.2:g.109814626A>G | GRCh38 |
| NC_000012.11:g.110252431A>G , CM000674.1:g.110252431A>G | GRCh37 |
| NC_000012.10:g.108736814A>G | NCBI36 |
| NG_017090.1:g.23782T>C , LRG_372:g.23782T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261740.7:c.171T>C MANE Select | ENSP00000261740.2:p.Pro57= | |
| ENST00000418703.7:c.171T>C | ENSP00000406191.2:p.Pro57= | |
| ENST00000674908.1:c.171T>C | ENSP00000502012.1:p.Pro57= | |
| ENST00000675533.1:n.202T>C | ||
| ENST00000675670.1:c.171T>C | ENSP00000502135.1:p.Pro57= | |
| ENST00000676376.1:n.202T>C | ||
| ENST00000261740.6:c.171T>C | ENSP00000261740.2:p.Pro57= | |
| ENST00000418703.6:c.171T>C | ENSP00000406191.2:p.Pro57= | |
| ENST00000536838.1:c.80-11T>C | ENSP00000444336.1:n.80-11T>C | |
| ENST00000537083.5:c.171T>C | ENSP00000442738.1:p.Pro57= | |
| ENST00000538125.5:c.171T>C | ENSP00000437449.1:p.Pro57= | |
| ENST00000541794.5:c.171T>C | ENSP00000442167.1:p.Pro57= | |
| ENST00000544971.5:c.171T>C | ENSP00000443611.1:p.Pro57= | |
| NM_001177428.1:c.171T>C | NP_001170899.1:p.Pro57= | |
| NM_001177431.1:c.80-11T>C | NP_001170902.1:n.80-11T>C | |
| NM_001177433.1:c.171T>C | NP_001170904.1:p.Pro57= | |
| NM_021625.4:c.171T>C , LRG_372t1:c.171T>C | NP_067638.3:p.Pro57= | |
| NM_147204.2:c.171T>C | NP_671737.1:p.Pro57= | |
| XM_005253918.1:c.171T>C | XP_005253975.1:p.Pro57= | |
| XM_011538630.1:c.171T>C | XP_011536932.1:p.Pro57= | |
| XM_011538631.1:c.171T>C | XP_011536933.1:p.Pro57= | |
| XM_011538632.1:c.171T>C | XP_011536934.1:p.Pro57= | |
| XM_011538633.1:c.171T>C | XP_011536935.1:p.Pro57= | |
| XM_011538634.1:c.171T>C | XP_011536936.1:p.Pro57= | |
| XM_011538635.1:c.324T>C | XP_011536937.1:p.Pro108= | |
| XM_011538636.1:c.324T>C | XP_011536938.1:p.Pro108= | |
| XM_011538630.2:c.324T>C | XP_011536932.2:p.Pro108= | |
| XM_011538631.2:c.324T>C | XP_011536933.2:p.Pro108= | |
| XM_011538632.2:c.324T>C | XP_011536934.2:p.Pro108= | |
| XM_011538633.2:c.324T>C | XP_011536935.2:p.Pro108= | |
| XM_011538634.2:c.324T>C | XP_011536936.2:p.Pro108= | |
| XM_011538635.2:c.324T>C | XP_011536937.1:p.Pro108= | |
| XM_017019774.1:c.171T>C | XP_016875263.1:p.Pro57= | |
| NM_021625.5:c.171T>C MANE Select | NP_067638.3:p.Pro57= |