Canonical Allele Identifier: CA1397901680

Gene: CSTA

Linked Data

• dbSNP Id: rs2075193909

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122329839C>G , CM000665.2:g.122329839C>G	GRCh38
NC_000003.11:g.122048686C>G , CM000665.1:g.122048686C>G	GRCh37
NC_000003.10:g.123531376C>G	NCBI36
NG_027995.1:g.9676C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264474.4:c.66+4481C>G MANE Select	ENSP00000264474.3:n.66+4481C>G
ENST00000264474.3:c.66+4481C>G	ENSP00000264474.3:n.66+4481C>G
ENST00000479204.1:c.66+4481C>G	ENSP00000418891.1:n.66+4481C>G
NM_005213.3:c.66+4481C>G	NP_005204.1:n.66+4481C>G
NM_005213.4:c.66+4481C>G MANE Select	NP_005204.1:n.66+4481C>G