Canonical Allele Identifier: CA1397901669

Gene: CSTA

Linked Data

• dbSNP Id: rs2075193801

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122329820G>C , CM000665.2:g.122329820G>C	GRCh38
NC_000003.11:g.122048667G>C , CM000665.1:g.122048667G>C	GRCh37
NC_000003.10:g.123531357G>C	NCBI36
NG_027995.1:g.9657G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264474.4:c.66+4462G>C MANE Select	ENSP00000264474.3:n.66+4462G>C
ENST00000264474.3:c.66+4462G>C	ENSP00000264474.3:n.66+4462G>C
ENST00000479204.1:c.66+4462G>C	ENSP00000418891.1:n.66+4462G>C
NM_005213.3:c.66+4462G>C	NP_005204.1:n.66+4462G>C
NM_005213.4:c.66+4462G>C MANE Select	NP_005204.1:n.66+4462G>C