Canonical Allele Identifier: CA1218511578
Gene:

Linked Data

dbSNP Id: rs1558164638

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198500099T>C , CM000663.2:g.198500099T>C GRCh38
NC_000001.10:g.198469229T>C , CM000663.1:g.198469229T>C GRCh37
NC_000001.9:g.196735852T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922398.1:n.679+19452A>G
XR_922398.2:n.341+19452A>G