Canonical Allele Identifier: CA2674169228
Gene: CARTPT HGNC NCBI

Linked Data

gnomAD v4: 5-71719267-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719267G>A , CM000667.2:g.71719267G>A GRCh38
NC_000005.9:g.71015094G>A , CM000667.1:g.71015094G>A GRCh37
NC_000005.8:g.71050850G>A NCBI36
NG_015988.1:g.5105G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.4:c.-27G>A ENSP00000296777.4:n.-27G>A
NM_004291.3:c.-27G>A NP_004282.1:n.-27G>A