Canonical Allele Identifier: CA996006583
Gene:

Linked Data

dbSNP Id: rs2071923083

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41648281A>G , CM000681.2:g.41648281A>G GRCh38
NC_000019.9:g.42152202A>G , CM000681.1:g.42152202A>G GRCh37
NC_000019.8:g.46844042A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935972.1:n.170+3221T>C