Canonical Allele Identifier: CA1374121524
Gene:

Linked Data

dbSNP Id: rs1704105316

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266711G>T , CM000665.2:g.72266711G>T GRCh38
NC_000003.11:g.72315862G>T , CM000665.1:g.72315862G>T GRCh37
NC_000003.10:g.72398552G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8397C>A