Canonical Allele Identifier: CA89976953
Gene:

Linked Data

dbSNP Id: rs957115190
gnomAD v2: 3-187649431-C-T
gnomAD v3: 3-187931643-C-T
gnomAD v4: 3-187931643-C-T
MyVariant Identifiers: chr3:g.187649431C>T (hg19) chr3:g.187931643C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.187931643C>T , CM000665.2:g.187931643C>T GRCh38
NC_000003.11:g.187649431C>T , CM000665.1:g.187649431C>T GRCh37
NC_000003.10:g.189132125C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924814.1:n.1271G>A
Search 100 bp 5'
Search 100 bp 3'