Canonical Allele Identifier: CA1000868308
Gene: PPT1 HGNC NCBI

Linked Data

dbSNP Id: rs757640604
gnomAD v3: 1-40097275-G-C
gnomAD v4: 1-40097275-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40097275G>C , CM000663.2:g.40097275G>C GRCh38
NC_000001.10:g.40562947G>C , CM000663.1:g.40562947G>C GRCh37
NC_000001.9:g.40335534G>C NCBI36
NG_009192.1:g.5196C>G , LRG_690:g.5196C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.7:c.-37C>G ENSP00000394863.3:n.-37C>G
NM_000310.3:c.-37C>G , LRG_690t1:c.-37C>G NP_000301.1:n.-37C>G
NM_001142604.1:c.-37C>G NP_001136076.1:n.-37C>G
NM_001363695.1:c.-37C>G NP_001350624.1:n.-37C>G
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