Canonical Allele Identifier: CA2695700005
Gene: PPT1 HGNC NCBI

Linked Data

dbSNP Id: rs2124494767

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40097286T>C , CM000663.2:g.40097286T>C GRCh38
NC_000001.10:g.40562958T>C , CM000663.1:g.40562958T>C GRCh37
NC_000001.9:g.40335545T>C NCBI36
NG_009192.1:g.5185A>G , LRG_690:g.5185A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.7:c.-48A>G ENSP00000394863.3:n.-48A>G
NM_000310.3:c.-48A>G , LRG_690t1:c.-48A>G NP_000301.1:n.-48A>G
NM_001142604.1:c.-48A>G NP_001136076.1:n.-48A>G
NM_001363695.1:c.-48A>G NP_001350624.1:n.-48A>G