Canonical Allele Identifier: CA2751871528
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079607G>T , CM000664.2:g.118079607G>T GRCh38
NC_000002.11:g.118837183G>T , CM000664.1:g.118837183G>T GRCh37
NC_000002.10:g.118553653G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512305.1:c.697-2075C>A XP_011510607.1:n.697-2075C>A
XR_001739662.2:n.138+8644C>A