Canonical Allele Identifier: CA2346122769
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470956A= , CM000682.2:g.2470956A= GRCh38
NC_000020.10:g.2451602A= , CM000682.1:g.2451602A= GRCh37
NC_000020.9:g.2399602A= NCBI36
NG_042057.1:g.4898T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3198T= ENSP00000456213.1:n.305-3198T=