Canonical Allele Identifier: CA15752950
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs1495377

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71183321G>C , CM000674.2:g.71183321G>C GRCh38
NC_000012.11:g.71577101G>C , CM000674.1:g.71577101G>C GRCh37
NC_000012.10:g.69863368G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393330.6:c.-109-25534C>G ENSP00000377003.2:p.=
ENST00000549421.1:n.207-25534C>G