Canonical Allele Identifier: CA735697703
Gene: PPT1 HGNC NCBI

Linked Data

dbSNP Id: rs1301807232
gnomAD v3: 1-40097419-C-A
gnomAD v4: 1-40097419-C-A
MyVariant Identifiers: chr1:g.40563091C>A (hg19) chr1:g.40097419C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40097419C>A , CM000663.2:g.40097419C>A GRCh38
NC_000001.10:g.40563091C>A , CM000663.1:g.40563091C>A GRCh37
NC_000001.9:g.40335678C>A NCBI36
NG_009192.1:g.5052G>T , LRG_690:g.5052G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.7:c.-181G>T ENSP00000394863.3:n.-181G>T
NM_000310.3:c.-181G>T , LRG_690t1:c.-181G>T NP_000301.1:n.-181G>T
NM_001142604.1:c.-181G>T NP_001136076.1:n.-181G>T
NM_001363695.1:c.-181G>T NP_001350624.1:n.-181G>T
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