Canonical Allele Identifier: CA2000590732
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166759T= , CM000673.2:g.112166759T= GRCh38
NC_000011.9:g.112037482T= , CM000673.1:g.112037482T= GRCh37
NC_000011.8:g.111542692T= NCBI36
NG_028143.1:g.2359A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525987.5:n.320-3660T=
ENST00000531744.5:c.315-3660T= ENSP00000456957.1:n.315-3660T=
ENST00000532699.1:c.315-3660T= ENSP00000456434.1:n.315-3660T=