Canonical Allele Identifier: CA2674169211
Gene: CARTPT HGNC NCBI

Linked Data

gnomAD v4: 5-71719243-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719243C>A , CM000667.2:g.71719243C>A GRCh38
NC_000005.9:g.71015070C>A , CM000667.1:g.71015070C>A GRCh37
NC_000005.8:g.71050826C>A NCBI36
NG_015988.1:g.5081C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.4:c.-51C>A ENSP00000296777.4:n.-51C>A
NM_004291.3:c.-51C>A NP_004282.1:n.-51C>A
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