Canonical Allele Identifier: CA2043864140
Gene:

Linked Data

dbSNP Id: rs1869799727

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68248118A>G , CM000674.2:g.68248118A>G GRCh38
NC_000012.11:g.68641898A>G , CM000674.1:g.68641898A>G GRCh37
NC_000012.10:g.66928165A>G NCBI36
NG_060763.1:g.10487T>C

Transcript Alleles

HGVS Amino-acid Change
XR_945055.1:n.265-16540A>G
XR_002957418.1:n.281-16540A>G