Canonical Allele Identifier: CA2581047036
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166661A>C , CM000673.2:g.112166661A>C GRCh38
NC_000011.9:g.112037384A>C , CM000673.1:g.112037384A>C GRCh37
NC_000011.8:g.111542594A>C NCBI36
NG_028143.1:g.2457T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000525987.5:n.320-3758A>C
ENST00000531744.5:c.315-3758A>C ENSP00000456957.1:n.315-3758A>C
ENST00000532699.1:c.315-3758A>C ENSP00000456434.1:n.315-3758A>C