Canonical Allele Identifier: CA354153067
Gene: CSTA HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.122060287T>A (hg19) chr3:g.122341440T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122341440T>A , CM000665.2:g.122341440T>A GRCh38
NC_000003.11:g.122060287T>A , CM000665.1:g.122060287T>A GRCh37
NC_000003.10:g.123542977T>A NCBI36
NG_027995.1:g.21277T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264474.4:c.170T>A MANE Select ENSP00000264474.3:p.Val57Glu
ENST00000264474.3:c.170T>A ENSP00000264474.3:p.Val57Glu
NM_005213.3:c.170T>A NP_005204.1:p.Val57Glu
NM_005213.4:c.170T>A MANE Select NP_005204.1:p.Val57Glu
Search 100 bp 5'
Search 100 bp 3'