Canonical Allele Identifier: CA881156398
Gene:

Linked Data

dbSNP Id: rs1313160000

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544694T>C , CM000681.2:g.28544694T>C GRCh38
NC_000019.9:g.29035601T>C , CM000681.1:g.29035601T>C GRCh37
NC_000019.8:g.33727441T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110759.1:n.657-77914A>G
XR_243979.1:n.110-51671A>G