Canonical Allele Identifier: CA2514124906
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2471013A>G , CM000682.2:g.2471013A>G GRCh38
NC_000020.10:g.2451659A>G , CM000682.1:g.2451659A>G GRCh37
NC_000020.9:g.2399659A>G NCBI36
NG_042057.1:g.4841T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3255T>C ENSP00000456213.1:n.305-3255T>C