Canonical Allele Identifier: CA1095881570
Gene:

Linked Data

dbSNP Id: rs1777130465

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151627278T>C , CM000668.2:g.151627278T>C GRCh38
NC_000006.11:g.151948413T>C , CM000668.1:g.151948413T>C GRCh37
NC_000006.10:g.151990106T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943113.1:n.704T>C
XR_943115.1:n.704T>C