Canonical Allele Identifier: CA1595576561
Gene:

Linked Data

dbSNP Id: rs2961920

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.160484499C>G , CM000667.2:g.160484499C>G GRCh38
NC_000005.9:g.159911506C>G , CM000667.1:g.159911506C>G GRCh37
NC_000005.8:g.159844084C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_132748.1:n.191-800C>G