Canonical Allele Identifier: CA2735724465
Gene:

Linked Data

dbSNP Id: rs2145087444

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544683C>G , CM000681.2:g.28544683C>G GRCh38
NC_000019.9:g.29035590C>G , CM000681.1:g.29035590C>G GRCh37
NC_000019.8:g.33727430C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110759.1:n.657-77903G>C
XR_243979.1:n.110-51660G>C