Canonical Allele Identifier: CA51878270
Gene:

Linked Data

dbSNP Id: rs1033313725

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016104A>T , CM000664.2:g.88016104A>T GRCh38
NC_000002.11:g.88315623A>T , CM000664.1:g.88315623A>T GRCh37
NC_000002.10:g.88096738A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.449A>T
XR_940336.3:n.449A>T