Linked Data
dbSNP Id:
rs11858577
gnomAD v2:
15-67066563-C-T
gnomAD v3:
15-66774225-C-T
gnomAD v4:
15-66774225-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.66774225C>T , CM000677.2:g.66774225C>T | GRCh38 |
| NC_000015.9:g.67066563C>T , CM000677.1:g.67066563C>T | GRCh37 |
| NC_000015.8:g.64853617C>T | NCBI36 |
| NG_012244.1:g.76890C>T | |
| NG_012244.2:g.76890C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000288840.10:c.953-6772C>T MANE Select | ENSP00000288840.5:n.953-6772C>T | |
| ENST00000288840.9:c.953-6772C>T | ENSP00000288840.5:n.953-6772C>T | |
| ENST00000557916.5:c.1085-6772C>T | ENSP00000452955.1:n.1085-6772C>T | |
| ENST00000559931.5:c.257-6772C>T | ENSP00000453446.1:n.257-6772C>T | |
| NM_005585.4:c.953-6772C>T | NP_005576.3:n.953-6772C>T | |
| NR_027654.1:n.2008-6772C>T | ||
| XM_011521561.1:c.170-6772C>T | XP_011519863.1:n.170-6772C>T | |
| XR_931825.1:n.2352-6772C>T | ||
| XM_011521561.2:c.170-6772C>T | XP_011519863.1:n.170-6772C>T | |
| NM_005585.5:c.953-6772C>T MANE Select | NP_005576.3:n.953-6772C>T | |
| NR_027654.2:n.2108-6772C>T |