Canonical Allele Identifier: CA2024154283
Gene:

Linked Data

dbSNP Id: rs1865524727

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.28045343A>G , CM000674.2:g.28045343A>G GRCh38
NC_000012.11:g.28198276A>G , CM000674.1:g.28198276A>G GRCh37
NC_000012.10:g.28089543A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931460.1:n.154-6385T>C