Canonical Allele Identifier: CA1573933691
Gene:

Linked Data

dbSNP Id: rs1780063214

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660999C>T , CM000667.2:g.113660999C>T GRCh38
NC_000005.9:g.112996696C>T , CM000667.1:g.112996696C>T GRCh37
NC_000005.8:g.113024595C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27635C>T