Canonical Allele Identifier: CA338565012
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15767022A>T (hg19) chr1:g.15440526A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15440526A>T , CM000663.2:g.15440526A>T GRCh38
NC_000001.10:g.15767022A>T , CM000663.1:g.15767022A>T GRCh37
NC_000001.9:g.15639609A>T NCBI36
NG_009253.1:g.7085A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.166A>T MANE Select ENSP00000365116.4:p.Arg56Trp
ENST00000375943.6:c.41-1921A>T ENSP00000365110.2:n.41-1921A>T
ENST00000375949.4:c.166A>T ENSP00000365116.4:p.Arg56Trp
ENST00000476813.5:n.53-1921A>T
ENST00000483406.1:n.76A>T
NM_007272.2:c.166A>T NP_009203.2:p.Arg56Trp
XM_011540550.1:c.166A>T XP_011538852.1:p.Arg56Trp
NM_007272.3:c.166A>T MANE Select NP_009203.2:p.Arg56Trp
Search 100 bp 5'
Search 100 bp 3'