Canonical Allele Identifier: CA338565034
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15767032G>C (hg19) chr1:g.15440536G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15440536G>C , CM000663.2:g.15440536G>C GRCh38
NC_000001.10:g.15767032G>C , CM000663.1:g.15767032G>C GRCh37
NC_000001.9:g.15639619G>C NCBI36
NG_009253.1:g.7095G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.176G>C MANE Select ENSP00000365116.4:p.Cys59Ser
ENST00000375943.6:c.41-1911G>C ENSP00000365110.2:n.41-1911G>C
ENST00000375949.4:c.176G>C ENSP00000365116.4:p.Cys59Ser
ENST00000476813.5:n.53-1911G>C
ENST00000483406.1:n.86G>C
NM_007272.2:c.176G>C NP_009203.2:p.Cys59Ser
XM_011540550.1:c.176G>C XP_011538852.1:p.Cys59Ser
NM_007272.3:c.176G>C MANE Select NP_009203.2:p.Cys59Ser
Search 100 bp 5'
Search 100 bp 3'