Canonical Allele Identifier: CA1672979329
Gene:

Linked Data

dbSNP Id: rs1777189270

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633775C>A , CM000668.2:g.151633775C>A GRCh38
NC_000006.11:g.151954910C>A , CM000668.1:g.151954910C>A GRCh37
NC_000006.10:g.151996603C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3793C>A