Linked Data
dbSNP Id:
rs980171881
gnomAD v2:
10-63747696-A-C
gnomAD v3:
10-61987937-A-C
gnomAD v4:
10-61987937-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.61987937A>C , CM000672.2:g.61987937A>C | GRCh38 |
| NC_000010.10:g.63747696A>C , CM000672.1:g.63747696A>C | GRCh37 |
| NC_000010.9:g.63417702A>C | NCBI36 |
| NG_030027.1:g.91684A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000279873.12:c.503-12154A>C MANE Select | ENSP00000279873.7:n.503-12154A>C | |
| ENST00000644638.1:c.503-12154A>C | ENSP00000494412.1:n.503-12154A>C | |
| ENST00000681100.1:c.503-12154A>C | ENSP00000506119.1:n.503-12154A>C | |
| ENST00000279873.11:c.503-12154A>C | ENSP00000279873.7:n.503-12154A>C | |
| NM_032199.2:c.503-12154A>C | NP_115575.1:n.503-12154A>C | |
| XM_011540262.1:c.502+47529A>C | XP_011538564.1:n.502+47529A>C | |
| XM_024448230.1:c.-65-12154A>C | XP_024303998.1:n.-65-12154A>C | |
| NM_032199.3:c.503-12154A>C MANE Select | NP_115575.1:n.503-12154A>C |