Canonical Allele Identifier: CA898128372
Gene: CSTA HGNC NCBI

Linked Data

dbSNP Id: rs1311967377
gnomAD v3: 3-122329727-G-T
gnomAD v4: 3-122329727-G-T
MyVariant Identifiers: chr3:g.122048574G>T (hg19) chr3:g.122329727G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122329727G>T , CM000665.2:g.122329727G>T GRCh38
NC_000003.11:g.122048574G>T , CM000665.1:g.122048574G>T GRCh37
NC_000003.10:g.123531264G>T NCBI36
NG_027995.1:g.9564G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264474.4:c.66+4369G>T MANE Select ENSP00000264474.3:n.66+4369G>T
ENST00000264474.3:c.66+4369G>T ENSP00000264474.3:n.66+4369G>T
ENST00000479204.1:c.66+4369G>T ENSP00000418891.1:n.66+4369G>T
NM_005213.3:c.66+4369G>T NP_005204.1:n.66+4369G>T
NM_005213.4:c.66+4369G>T MANE Select NP_005204.1:n.66+4369G>T
Search 100 bp 5'
Search 100 bp 3'