Canonical Allele Identifier: CA11066311
Community Standard Title: NC_000002.12:g.46617108G>T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46617108G>T , CM000664.2:g.46617108G>T GRCh38
NC_000002.11:g.46844247G>T , CM000664.1:g.46844247G>T GRCh37
NC_000002.10:g.46697751G>T NCBI36
NG_034144.1:g.4937G>T

Transcript Alleles

HGVS Amino-acid Change
NM_002643.3:c.-160C>A (PIGF) NP_002634.1:n.-160C>A
NM_173074.2:c.-160C>A (PIGF) NP_775097.1:n.-160C>A
ENST00000281382.10:c.-160C>A (PIGF) ENSP00000281382.6:n.-160C>A
ENST00000486447.1:n.608+85G>T (CRIPT)