Canonical Allele Identifier: CA2667232086
Gene: CSTA HGNC NCBI

Linked Data

gnomAD v4: 3-122325256-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122325256T>A , CM000665.2:g.122325256T>A GRCh38
NC_000003.11:g.122044103T>A , CM000665.1:g.122044103T>A GRCh37
NC_000003.10:g.123526793T>A NCBI36
NG_027995.1:g.5093T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264474.4:c.-37T>A MANE Select ENSP00000264474.3:n.-37T>A
ENST00000264474.3:c.-37T>A ENSP00000264474.3:n.-37T>A
NM_005213.3:c.-37T>A NP_005204.1:n.-37T>A
NM_005213.4:c.-37T>A MANE Select NP_005204.1:n.-37T>A
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