Canonical Allele Identifier: CA354153071

Gene: CSTA

Linked Data

• MyVariant Identifiers: chr3:g.122060289C>G (hg19) ; chr3:g.122341442C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122341442C>G , CM000665.2:g.122341442C>G	GRCh38
NC_000003.11:g.122060289C>G , CM000665.1:g.122060289C>G	GRCh37
NC_000003.10:g.123542979C>G	NCBI36
NG_027995.1:g.21279C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264474.4:c.172C>G MANE Select	ENSP00000264474.3:p.Arg58Gly
ENST00000264474.3:c.172C>G	ENSP00000264474.3:p.Arg58Gly
NM_005213.3:c.172C>G	NP_005204.1:p.Arg58Gly
NM_005213.4:c.172C>G MANE Select	NP_005204.1:p.Arg58Gly