Canonical Allele Identifier: CA2674169215
Gene: CARTPT HGNC NCBI

Linked Data

gnomAD v4: 5-71719253-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719253T>C , CM000667.2:g.71719253T>C GRCh38
NC_000005.9:g.71015080T>C , CM000667.1:g.71015080T>C GRCh37
NC_000005.8:g.71050836T>C NCBI36
NG_015988.1:g.5091T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.4:c.-41T>C ENSP00000296777.4:n.-41T>C
NM_004291.3:c.-41T>C NP_004282.1:n.-41T>C
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