Canonical Allele Identifier: CA64382867
Gene:

Linked Data

dbSNP Id: rs576861002

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033103G>T , CM000664.2:g.200033103G>T GRCh38
NC_000002.11:g.200897826G>T , CM000664.1:g.200897826G>T GRCh37
NC_000002.10:g.200606071G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923778.1:n.178-22207C>A