Canonical Allele Identifier: CA1573933710
Gene:

Linked Data

dbSNP Id: rs1780063540

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113661073T>C , CM000667.2:g.113661073T>C GRCh38
NC_000005.9:g.112996770T>C , CM000667.1:g.112996770T>C GRCh37
NC_000005.8:g.113024669T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27709T>C