Canonical Allele Identifier: CA14498517
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10048158

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240200T>C , CM000679.2:g.66240200T>C GRCh38
NC_000017.9:g.61666780T>C NCBI36
NC_000017.10:g.64236318T>C , CM000679.1:g.64236318T>C GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10778A>G ENSP00000464301.1:p.=