Canonical Allele Identifier: CA1397899533
Gene: CSTA HGNC NCBI

Linked Data

dbSNP Id: rs2075164467
gnomAD v4: 3-122325277-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122325277G>A , CM000665.2:g.122325277G>A GRCh38
NC_000003.11:g.122044124G>A , CM000665.1:g.122044124G>A GRCh37
NC_000003.10:g.123526814G>A NCBI36
NG_027995.1:g.5114G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264474.4:c.-16G>A MANE Select ENSP00000264474.3:n.-16G>A
ENST00000264474.3:c.-16G>A ENSP00000264474.3:n.-16G>A
ENST00000479204.1:c.-16G>A ENSP00000418891.1:n.-16G>A
NM_005213.3:c.-16G>A NP_005204.1:n.-16G>A
NM_005213.4:c.-16G>A MANE Select NP_005204.1:n.-16G>A
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