Canonical Allele Identifier: CA1213147497

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186453331C= , CM000663.2:g.186453331C= GRCh38
NC_000001.10:g.186422463C= , CM000663.1:g.186422463C= GRCh37
NC_000001.9:g.184689086C= NCBI36
NG_009101.1:g.12777G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000391997.3:c.-24-3848G= (PDC) MANE Select ENSP00000375855.2:n.-24-3848G=
ENST00000391997.2:c.-24-3848G= (PDC) ENSP00000375855.2:n.-24-3848G=
NM_002597.4:c.-24-3848G= (PDC) NP_002588.3:n.-24-3848G=
NR_126002.1:n.441+2057C= (PDC-AS1)
NM_002597.5:c.-24-3848G= (PDC) MANE Select NP_002588.3:n.-24-3848G=