Canonical Allele Identifier: CA1439212648
Gene:

Linked Data

dbSNP Id: rs1560232866

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578035A>G , CM000666.2:g.12578035A>G GRCh38
NC_000004.11:g.12579659A>G , CM000666.1:g.12579659A>G GRCh37
NC_000004.10:g.12188757A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31307T>C
XR_001741374.1:n.254+44620T>C
XR_925406.3:n.140+31307T>C