Canonical Allele Identifier: CA59107089
Gene:

Linked Data

dbSNP Id: rs1037693725

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870621C>G , CM000664.2:g.155870621C>G GRCh38
NC_000002.11:g.156727133C>G , CM000664.1:g.156727133C>G GRCh37
NC_000002.10:g.156435379C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3434G>C
XR_001739749.1:n.331-29637G>C
XR_001739750.1:n.331-29637G>C
XR_001739751.1:n.331-29637G>C
XR_923501.2:n.331-3434G>C