Canonical Allele Identifier: CA2581047038
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166930G>C , CM000673.2:g.112166930G>C GRCh38
NC_000011.9:g.112037653G>C , CM000673.1:g.112037653G>C GRCh37
NC_000011.8:g.111542863G>C NCBI36
NG_028143.1:g.2188C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000525987.5:n.320-3489G>C
ENST00000531744.5:c.315-3489G>C ENSP00000456957.1:n.315-3489G>C
ENST00000532699.1:c.315-3489G>C ENSP00000456434.1:n.315-3489G>C