Canonical Allele Identifier: CA1300258797
Gene:

Linked Data

dbSNP Id: rs1683148739

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870604T>G , CM000664.2:g.155870604T>G GRCh38
NC_000002.11:g.156727116T>G , CM000664.1:g.156727116T>G GRCh37
NC_000002.10:g.156435362T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3417A>C
XR_001739749.1:n.331-29620A>C
XR_001739750.1:n.331-29620A>C
XR_001739751.1:n.331-29620A>C
XR_923501.2:n.331-3417A>C