Canonical Allele Identifier: CA338565089
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15767058T>C (hg19) chr1:g.15440562T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15440562T>C , CM000663.2:g.15440562T>C GRCh38
NC_000001.10:g.15767058T>C , CM000663.1:g.15767058T>C GRCh37
NC_000001.9:g.15639645T>C NCBI36
NG_009253.1:g.7121T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.202T>C MANE Select ENSP00000365116.4:p.Phe68Leu
ENST00000375943.6:c.41-1885T>C ENSP00000365110.2:n.41-1885T>C
ENST00000375949.4:c.202T>C ENSP00000365116.4:p.Phe68Leu
ENST00000476813.5:n.53-1885T>C
ENST00000483406.1:n.112T>C
NM_007272.2:c.202T>C NP_009203.2:p.Phe68Leu
XM_011540550.1:c.202T>C XP_011538852.1:p.Phe68Leu
NM_007272.3:c.202T>C MANE Select NP_009203.2:p.Phe68Leu
Search 100 bp 5'
Search 100 bp 3'