Linked Data
dbSNP Id:
rs1173577945
gnomAD v2:
5-156486313-G-A
gnomAD v3:
5-157059302-G-A
gnomAD v4:
5-157059302-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157059302G>A , CM000667.2:g.157059302G>A | GRCh38 |
| NC_000005.9:g.156486313G>A , CM000667.1:g.156486313G>A | GRCh37 |
| NC_000005.8:g.156418891G>A | NCBI36 |
| NG_017001.1:g.4658C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699093.1:c.-12-1347C>T | ENSP00000514125.1:n.-12-1347C>T | |
| XM_011534511.1:c.-133-1226C>T | XP_011532813.1:n.-133-1226C>T | |
| XM_011534513.1:c.-12-1347C>T | XP_011532815.1:n.-12-1347C>T | |
| XM_024446020.1:c.-136-1223C>T | XP_024301788.1:n.-136-1223C>T | |
| XM_024446021.1:c.-133-1226C>T | XP_024301789.1:n.-133-1226C>T | |
| XM_024446023.1:c.-12-1347C>T | XP_024301791.1:n.-12-1347C>T |