Canonical Allele Identifier: CA881156386
Gene:

Linked Data

dbSNP Id: rs1320843870

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544690A>C , CM000681.2:g.28544690A>C GRCh38
NC_000019.9:g.29035597A>C , CM000681.1:g.29035597A>C GRCh37
NC_000019.8:g.33727437A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110759.1:n.657-77910T>G
XR_243979.1:n.110-51667T>G