Canonical Allele Identifier: CA1320446076
Gene:

Linked Data

dbSNP Id: rs2077888432

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033035G>T , CM000664.2:g.200033035G>T GRCh38
NC_000002.11:g.200897758G>T , CM000664.1:g.200897758G>T GRCh37
NC_000002.10:g.200606003G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22139C>A