Canonical Allele Identifier: CA2566921886
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166845A>G , CM000673.2:g.112166845A>G GRCh38
NC_000011.9:g.112037568A>G , CM000673.1:g.112037568A>G GRCh37
NC_000011.8:g.111542778A>G NCBI36
NG_028143.1:g.2273T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3574A>G
ENST00000531744.5:c.315-3574A>G ENSP00000456957.1:n.315-3574A>G
ENST00000532699.1:c.315-3574A>G ENSP00000456434.1:n.315-3574A>G