Canonical Allele Identifier: CA1048602074
Gene:

Linked Data

dbSNP Id: rs2041753402
gnomAD v3: 3-61428152-T-C
gnomAD v4: 3-61428152-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428152T>C , CM000665.2:g.61428152T>C GRCh38
NC_000003.11:g.61413826T>C , CM000665.1:g.61413826T>C GRCh37
NC_000003.10:g.61388866T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.164+362A>G
XR_940893.1:n.164+362A>G
XR_001740725.1:n.202+362A>G
XR_940892.2:n.202+362A>G