Canonical Allele Identifier: CA1167208792
Gene: CPT2 HGNC NCBI

Linked Data

dbSNP Id: rs1572378011
gnomAD v4: 1-53196723-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196723C>G , CM000663.2:g.53196723C>G GRCh38
NC_000001.10:g.53662395C>G , CM000663.1:g.53662395C>G GRCh37
NC_000001.9:g.53434983C>G NCBI36
NG_008035.1:g.5295C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-221C>G ENSP00000360541.3:n.-221C>G
NM_000098.2:c.-221C>G NP_000089.1:n.-221C>G
NM_001330589.1:c.-221C>G NP_001317518.1:n.-221C>G
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