Linked Data
dbSNP Id:
rs976061203
gnomAD v2:
1-17313288-C-T
gnomAD v3:
1-16986793-C-T
gnomAD v4:
1-16986793-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.16986793C>T , CM000663.2:g.16986793C>T | GRCh38 |
| NC_000001.10:g.17313288C>T , CM000663.1:g.17313288C>T | GRCh37 |
| NC_000001.9:g.17185875C>T | NCBI36 |
| NG_009054.1:g.30136G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000326735.13:c.3235+12G>A MANE Select | ENSP00000327214.8:n.3235+12G>A | |
| ENST00000326735.12:c.3235+12G>A | ENSP00000327214.8:n.3235+12G>A | |
| ENST00000341676.9:c.3103+12G>A | ENSP00000341115.5:n.3103+12G>A | |
| ENST00000452699.5:c.3220+12G>A | ENSP00000413307.1:n.3220+12G>A | |
| ENST00000466561.1:n.1121G>A | ||
| ENST00000502418.1:c.823+12G>A | ENSP00000423065.1:n.823+12G>A | |
| NM_001141973.2:c.3220+12G>A | NP_001135445.1:n.3220+12G>A | |
| NM_001141974.2:c.3103+12G>A | NP_001135446.1:n.3103+12G>A | |
| NM_022089.3:c.3235+12G>A | NP_071372.1:n.3235+12G>A | |
| XM_005245809.1:c.3235+12G>A | XP_005245866.1:n.3235+12G>A | |
| XM_005245810.1:c.3232+12G>A | XP_005245867.1:n.3232+12G>A | |
| XM_005245811.1:c.3220+12G>A | XP_005245868.1:n.3220+12G>A | |
| XM_005245812.1:c.3208+12G>A | XP_005245869.1:n.3208+12G>A | |
| XM_005245813.1:c.3175+12G>A | XP_005245870.1:n.3175+12G>A | |
| XM_005245815.1:c.3118+12G>A | XP_005245872.1:n.3118+12G>A | |
| XM_006710512.1:c.3217+12G>A | XP_006710575.1:n.3217+12G>A | |
| XM_006710513.1:c.3193+12G>A | XP_006710576.1:n.3193+12G>A | |
| XM_011541128.1:c.3220+12G>A | XP_011539430.1:n.3220+12G>A | |
| XM_011541129.1:c.3028+12G>A | XP_011539431.1:n.3028+12G>A | |
| XM_017000844.1:c.3220+12G>A | XP_016856333.1:n.3220+12G>A | |
| XM_017000845.1:c.3217+12G>A | XP_016856334.1:n.3217+12G>A | |
| XM_017000846.1:c.3193+12G>A | XP_016856335.1:n.3193+12G>A | |
| XM_017000847.1:c.3190+12G>A | XP_016856336.1:n.3190+12G>A | |
| XM_017000848.1:c.3118+12G>A | XP_016856337.1:n.3118+12G>A | |
| XM_017000849.1:c.3103+12G>A | XP_016856338.1:n.3103+12G>A | |
| XM_017000850.1:c.3028+12G>A | XP_016856339.1:n.3028+12G>A | |
| NM_022089.4:c.3235+12G>A MANE Select | NP_071372.1:n.3235+12G>A | |
| NM_001141973.3:c.3220+12G>A | NP_001135445.1:n.3220+12G>A | |
| NM_001141974.3:c.3103+12G>A | NP_001135446.1:n.3103+12G>A |