Canonical Allele Identifier: CA1615804255
Gene:

Linked Data

dbSNP Id: rs1762375537

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.23076999C>T , CM000668.2:g.23076999C>T GRCh38
NC_000006.11:g.23077227C>T , CM000668.1:g.23077227C>T GRCh37
NC_000006.10:g.23185206C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926583.1:n.246-19932G>A
XR_926584.1:n.246-60179G>A
XR_926583.2:n.246-19932G>A