Canonical Allele Identifier: CA2674169230
Gene: CARTPT HGNC NCBI

Linked Data

gnomAD v4: 5-71719268-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719268C>G , CM000667.2:g.71719268C>G GRCh38
NC_000005.9:g.71015095C>G , CM000667.1:g.71015095C>G GRCh37
NC_000005.8:g.71050851C>G NCBI36
NG_015988.1:g.5106C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.4:c.-26C>G ENSP00000296777.4:n.-26C>G
NM_004291.3:c.-26C>G NP_004282.1:n.-26C>G