Canonical Allele Identifier: CA2491383687
Gene:

Linked Data

dbSNP Id: rs1305459270

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458355A>G , CM000664.2:g.16458355A>G GRCh38
NC_000002.11:g.16639623A>G , CM000664.1:g.16639623A>G GRCh37
NC_000002.10:g.16503104A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939752.1:n.396-3261T>C