Canonical Allele Identifier: CA2492005149
Gene:

Linked Data

dbSNP Id: rs1673966391

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17843914A>G , CM000664.2:g.17843914A>G GRCh38
NC_000002.11:g.18025181A>G , CM000664.1:g.18025181A>G GRCh37
NC_000002.10:g.17888662A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3780T>C