Canonical Allele Identifier: CA898126918
Gene: CSTA HGNC NCBI

Linked Data

dbSNP Id: rs1251205365
gnomAD v3: 3-122325266-T-G
gnomAD v4: 3-122325266-T-G
MyVariant Identifiers: chr3:g.122044113T>G (hg19) chr3:g.122325266T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122325266T>G , CM000665.2:g.122325266T>G GRCh38
NC_000003.11:g.122044113T>G , CM000665.1:g.122044113T>G GRCh37
NC_000003.10:g.123526803T>G NCBI36
NG_027995.1:g.5103T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264474.4:c.-27T>G MANE Select ENSP00000264474.3:n.-27T>G
ENST00000264474.3:c.-27T>G ENSP00000264474.3:n.-27T>G
ENST00000479204.1:c.-27T>G ENSP00000418891.1:n.-27T>G
NM_005213.3:c.-27T>G NP_005204.1:n.-27T>G
NM_005213.4:c.-27T>G MANE Select NP_005204.1:n.-27T>G
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