Canonical Allele Identifier: CA1672973832
Gene:

Linked Data

dbSNP Id: rs1777129179

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151627168C>T , CM000668.2:g.151627168C>T GRCh38
NC_000006.11:g.151948303C>T , CM000668.1:g.151948303C>T GRCh37
NC_000006.10:g.151989996C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943113.1:n.594C>T
XR_943115.1:n.594C>T