Canonical Allele Identifier: CA354153051
Gene: CSTA HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.122060284A>C (hg19) chr3:g.122341437A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122341437A>C , CM000665.2:g.122341437A>C GRCh38
NC_000003.11:g.122060284A>C , CM000665.1:g.122060284A>C GRCh37
NC_000003.10:g.123542974A>C NCBI36
NG_027995.1:g.21274A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264474.4:c.169-2A>C MANE Select ENSP00000264474.3:n.169-2A>C
ENST00000264474.3:c.169-2A>C ENSP00000264474.3:n.169-2A>C
NM_005213.3:c.169-2A>C NP_005204.1:n.169-2A>C
NM_005213.4:c.169-2A>C MANE Select NP_005204.1:n.169-2A>C
Search 100 bp 5'
Search 100 bp 3'