Canonical Allele Identifier: CA1213147489

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186453313G= , CM000663.2:g.186453313G= GRCh38
NC_000001.10:g.186422445G= , CM000663.1:g.186422445G= GRCh37
NC_000001.9:g.184689068G= NCBI36
NG_009101.1:g.12795C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000391997.3:c.-24-3830C= (PDC) MANE Select ENSP00000375855.2:n.-24-3830C=
ENST00000391997.2:c.-24-3830C= (PDC) ENSP00000375855.2:n.-24-3830C=
NM_002597.4:c.-24-3830C= (PDC) NP_002588.3:n.-24-3830C=
NR_126002.1:n.441+2039G= (PDC-AS1)
NM_002597.5:c.-24-3830C= (PDC) MANE Select NP_002588.3:n.-24-3830C=