Canonical Allele Identifier: CA2024154245
Gene:

Linked Data

dbSNP Id: rs1231397543

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.28045234T>C , CM000674.2:g.28045234T>C GRCh38
NC_000012.11:g.28198167T>C , CM000674.1:g.28198167T>C GRCh37
NC_000012.10:g.28089434T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931460.1:n.154-6276A>G