Linked Data
dbSNP Id:
rs146884019
ExAC:
1:17313404 T / C
gnomAD v2:
1-17313404-T-C
gnomAD v3:
1-16986909-T-C
gnomAD v4:
1-16986909-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.16986909T>C , CM000663.2:g.16986909T>C | GRCh38 |
| NC_000001.10:g.17313404T>C , CM000663.1:g.17313404T>C | GRCh37 |
| NC_000001.9:g.17185991T>C | NCBI36 |
| NG_009054.1:g.30020A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326735.13:c.3131A>G MANE Select | ENSP00000327214.8:p.Asn1044Ser | |
| ENST00000326735.12:c.3131A>G | ENSP00000327214.8:p.Asn1044Ser | |
| ENST00000341676.9:c.2999A>G | ENSP00000341115.5:p.Asn1000Ser | |
| ENST00000452699.5:c.3116A>G | ENSP00000413307.1:p.Asn1039Ser | |
| ENST00000466561.1:n.1005A>G | ||
| ENST00000502418.1:c.719A>G | ENSP00000423065.1:p.Asn240Ser | |
| NM_001141973.2:c.3116A>G | NP_001135445.1:p.Asn1039Ser | |
| NM_001141974.2:c.2999A>G | NP_001135446.1:p.Asn1000Ser | |
| NM_022089.3:c.3131A>G | NP_071372.1:p.Asn1044Ser | |
| XM_005245809.1:c.3131A>G | XP_005245866.1:p.Asn1044Ser | |
| XM_005245810.1:c.3128A>G | XP_005245867.1:p.Asn1043Ser | |
| XM_005245811.1:c.3116A>G | XP_005245868.1:p.Asn1039Ser | |
| XM_005245812.1:c.3104A>G | XP_005245869.1:p.Asn1035Ser | |
| XM_005245813.1:c.3071A>G | XP_005245870.1:p.Asn1024Ser | |
| XM_005245815.1:c.3014A>G | XP_005245872.1:p.Asn1005Ser | |
| XM_006710512.1:c.3113A>G | XP_006710575.1:p.Asn1038Ser | |
| XM_006710513.1:c.3089A>G | XP_006710576.1:p.Asn1030Ser | |
| XM_011541128.1:c.3116A>G | XP_011539430.1:p.Asn1039Ser | |
| XM_011541129.1:c.2924A>G | XP_011539431.1:p.Asn975Ser | |
| XM_017000844.1:c.3116A>G | XP_016856333.1:p.Asn1039Ser | |
| XM_017000845.1:c.3113A>G | XP_016856334.1:p.Asn1038Ser | |
| XM_017000846.1:c.3089A>G | XP_016856335.1:p.Asn1030Ser | |
| XM_017000847.1:c.3086A>G | XP_016856336.1:p.Asn1029Ser | |
| XM_017000848.1:c.3014A>G | XP_016856337.1:p.Asn1005Ser | |
| XM_017000849.1:c.2999A>G | XP_016856338.1:p.Asn1000Ser | |
| XM_017000850.1:c.2924A>G | XP_016856339.1:p.Asn975Ser | |
| NM_022089.4:c.3131A>G MANE Select | NP_071372.1:p.Asn1044Ser | |
| NM_001141973.3:c.3116A>G | NP_001135445.1:p.Asn1039Ser | |
| NM_001141974.3:c.2999A>G | NP_001135446.1:p.Asn1000Ser |