Canonical Allele Identifier: CA545644762
Gene: CSTA HGNC NCBI

Linked Data

dbSNP Id: rs1484148284
gnomAD v2: 3-122044117-C-T
gnomAD v4: 3-122325270-C-T
MyVariant Identifiers: chr3:g.122044117C>T (hg19) chr3:g.122325270C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122325270C>T , CM000665.2:g.122325270C>T GRCh38
NC_000003.11:g.122044117C>T , CM000665.1:g.122044117C>T GRCh37
NC_000003.10:g.123526807C>T NCBI36
NG_027995.1:g.5107C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264474.4:c.-23C>T MANE Select ENSP00000264474.3:n.-23C>T
ENST00000264474.3:c.-23C>T ENSP00000264474.3:n.-23C>T
ENST00000479204.1:c.-23C>T ENSP00000418891.1:n.-23C>T
NM_005213.3:c.-23C>T NP_005204.1:n.-23C>T
NM_005213.4:c.-23C>T MANE Select NP_005204.1:n.-23C>T
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