Canonical Allele Identifier: CA338567802
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15772153T>C (hg19) chr1:g.15445658T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445658T>C , CM000663.2:g.15445658T>C GRCh38
NC_000001.10:g.15772153T>C , CM000663.1:g.15772153T>C GRCh37
NC_000001.9:g.15644740T>C NCBI36
NG_009253.1:g.12216T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.701T>C MANE Select ENSP00000365116.4:p.Ile234Thr
ENST00000375943.6:c.*155T>C ENSP00000365110.2:n.*155T>C
ENST00000375949.4:c.701T>C ENSP00000365116.4:p.Ile234Thr
ENST00000483406.1:n.465T>C
NM_007272.2:c.701T>C NP_009203.2:p.Ile234Thr
XM_011540550.1:c.555T>C XP_011538852.1:p.His185=
NM_007272.3:c.701T>C MANE Select NP_009203.2:p.Ile234Thr
Search 100 bp 5'
Search 100 bp 3'