Canonical Allele Identifier: CA2751927279
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120331877G>T , CM000664.2:g.120331877G>T GRCh38
NC_000002.11:g.121089453G>T , CM000664.1:g.121089453G>T GRCh37
NC_000002.10:g.120805923G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512307.1:c.141+3071G>T XP_011510609.1:n.141+3071G>T