Canonical Allele Identifier: CA338565084
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15767056A>C (hg19) chr1:g.15440560A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15440560A>C , CM000663.2:g.15440560A>C GRCh38
NC_000001.10:g.15767056A>C , CM000663.1:g.15767056A>C GRCh37
NC_000001.9:g.15639643A>C NCBI36
NG_009253.1:g.7119A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.200A>C MANE Select ENSP00000365116.4:p.Asn67Thr
ENST00000375943.6:c.41-1887A>C ENSP00000365110.2:n.41-1887A>C
ENST00000375949.4:c.200A>C ENSP00000365116.4:p.Asn67Thr
ENST00000476813.5:n.53-1887A>C
ENST00000483406.1:n.110A>C
NM_007272.2:c.200A>C NP_009203.2:p.Asn67Thr
XM_011540550.1:c.200A>C XP_011538852.1:p.Asn67Thr
NM_007272.3:c.200A>C MANE Select NP_009203.2:p.Asn67Thr
Search 100 bp 5'
Search 100 bp 3'