Canonical Allele Identifier: CA1167208754

Gene: CPT2

Linked Data

• dbSNP Id: rs1448651916
• gnomAD v4: 1-53196685-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53196685G>T , CM000663.2:g.53196685G>T	GRCh38
NC_000001.10:g.53662357G>T , CM000663.1:g.53662357G>T	GRCh37
NC_000001.9:g.53434945G>T	NCBI36
NG_008035.1:g.5257G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.3:c.-259G>T	ENSP00000360541.3:n.-259G>T
NM_000098.2:c.-259G>T	NP_000089.1:n.-259G>T
NM_001330589.1:c.-259G>T	NP_001317518.1:n.-259G>T