Canonical Allele Identifier: CA1095881533
Gene:

Linked Data

dbSNP Id: rs2039578455

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151627153C>T , CM000668.2:g.151627153C>T GRCh38
NC_000006.11:g.151948288C>T , CM000668.1:g.151948288C>T GRCh37
NC_000006.10:g.151989981C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943113.1:n.579C>T
XR_943115.1:n.579C>T