Canonical Allele Identifier: CA338567896
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15772201T>A (hg19) chr1:g.15445706T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445706T>A , CM000663.2:g.15445706T>A GRCh38
NC_000001.10:g.15772201T>A , CM000663.1:g.15772201T>A GRCh37
NC_000001.9:g.15644788T>A NCBI36
NG_009253.1:g.12264T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.749T>A MANE Select ENSP00000365116.4:p.Val250Glu
ENST00000375943.6:c.*203T>A ENSP00000365110.2:n.*203T>A
ENST00000375949.4:c.749T>A ENSP00000365116.4:p.Val250Glu
ENST00000483406.1:n.513T>A
NM_007272.2:c.749T>A NP_009203.2:p.Val250Glu
XM_011540550.1:c.603T>A XP_011538852.1:p.Gly201=
NM_007272.3:c.749T>A MANE Select NP_009203.2:p.Val250Glu
Search 100 bp 5'
Search 100 bp 3'