Canonical Allele Identifier: CA1038177555
Gene:

Linked Data

dbSNP Id: rs1683148241

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870582A>G , CM000664.2:g.155870582A>G GRCh38
NC_000002.11:g.156727094A>G , CM000664.1:g.156727094A>G GRCh37
NC_000002.10:g.156435340A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3395T>C
XR_001739749.1:n.331-29598T>C
XR_001739750.1:n.331-29598T>C
XR_001739751.1:n.331-29598T>C
XR_923501.2:n.331-3395T>C