Canonical Allele Identifier: CA998927574
Gene: CTRC HGNC NCBI

Linked Data

dbSNP Id: rs1708211807
gnomAD v4: 1-15445887-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445887C>T , CM000663.2:g.15445887C>T GRCh38
NC_000001.10:g.15772382C>T , CM000663.1:g.15772382C>T GRCh37
NC_000001.9:g.15644969C>T NCBI36
NG_009253.1:g.12445C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+138C>T MANE Select ENSP00000365116.4:n.792+138C>T
ENST00000375943.6:c.*246+138C>T ENSP00000365110.2:n.*246+138C>T
ENST00000375949.4:c.792+138C>T ENSP00000365116.4:n.792+138C>T
ENST00000483406.1:n.556+138C>T
NM_007272.2:c.792+138C>T NP_009203.2:n.792+138C>T
XM_011540550.1:c.646+138C>T XP_011538852.1:n.646+138C>T
NM_007272.3:c.792+138C>T MANE Select NP_009203.2:n.792+138C>T
Search 100 bp 5'
Search 100 bp 3'