Canonical Allele Identifier: CA1619157031
Gene:

Linked Data

dbSNP Id: rs981939551

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439680A>G , CM000668.2:g.31439680A>G GRCh38
NC_000006.11:g.31407457A>G , CM000668.1:g.31407457A>G GRCh37
NC_000006.10:g.31515436A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.427T>C