Canonical Allele Identifier: CA338567698
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15772107C>A (hg19) chr1:g.15445612C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445612C>A , CM000663.2:g.15445612C>A GRCh38
NC_000001.10:g.15772107C>A , CM000663.1:g.15772107C>A GRCh37
NC_000001.9:g.15644694C>A NCBI36
NG_009253.1:g.12170C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.655C>A MANE Select ENSP00000365116.4:p.Pro219Thr
ENST00000375943.6:c.*109C>A ENSP00000365110.2:n.*109C>A
ENST00000375949.4:c.655C>A ENSP00000365116.4:p.Pro219Thr
ENST00000483406.1:n.419C>A
NM_007272.2:c.655C>A NP_009203.2:p.Pro219Thr
XM_011540550.1:c.509C>A XP_011538852.1:p.Pro170His
NM_007272.3:c.655C>A MANE Select NP_009203.2:p.Pro219Thr
Search 100 bp 5'
Search 100 bp 3'