Canonical Allele Identifier: CA188145831
Gene:

Linked Data

dbSNP Id: rs536964968
gnomAD v2: 9-1787371-G-T
gnomAD v3: 9-1787371-G-T
gnomAD v4: 9-1787371-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787371G>T , CM000671.2:g.1787371G>T GRCh38
NC_000009.11:g.1787371G>T , CM000671.1:g.1787371G>T GRCh37
NC_000009.10:g.1777371G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68459G>T