Canonical Allele Identifier: CA76316061
Gene:

Linked Data

dbSNP Id: rs557087355
gnomAD v3: 3-61428155-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428155G>T , CM000665.2:g.61428155G>T GRCh38
NC_000003.11:g.61413829G>T , CM000665.1:g.61413829G>T GRCh37
NC_000003.10:g.61388869G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.164+359C>A
XR_940893.1:n.164+359C>A
XR_001740725.1:n.202+359C>A
XR_940892.2:n.202+359C>A