Canonical Allele Identifier: CA2506166347
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499867T>C , CM000666.2:g.102499867T>C GRCh38
NC_000004.11:g.103421024T>C , CM000666.1:g.103421024T>C GRCh37
NC_000004.10:g.103640056T>C NCBI36
NG_050628.1:g.3539T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1382A>G XP_011530769.1:n.643+1382A>G
NR_136202.1:n.48+2572A>G