Canonical Allele Identifier: CA338567819
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15772161T>A (hg19) chr1:g.15445666T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445666T>A , CM000663.2:g.15445666T>A GRCh38
NC_000001.10:g.15772161T>A , CM000663.1:g.15772161T>A GRCh37
NC_000001.9:g.15644748T>A NCBI36
NG_009253.1:g.12224T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.709T>A MANE Select ENSP00000365116.4:p.Phe237Ile
ENST00000375943.6:c.*163T>A ENSP00000365110.2:n.*163T>A
ENST00000375949.4:c.709T>A ENSP00000365116.4:p.Phe237Ile
ENST00000483406.1:n.473T>A
NM_007272.2:c.709T>A NP_009203.2:p.Phe237Ile
XM_011540550.1:c.563T>A XP_011538852.1:p.Leu188His
NM_007272.3:c.709T>A MANE Select NP_009203.2:p.Phe237Ile
Search 100 bp 5'
Search 100 bp 3'