Canonical Allele Identifier: CA613478
Gene: CTRC HGNC NCBI

Linked Data

dbSNP Id: rs761777960
ExAC: 1:15772272 G / A
gnomAD v2: 1-15772272-G-A
MyVariant Identifiers: chr1:g.15772272G>A (hg19) chr1:g.15445777G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445777G>A , CM000663.2:g.15445777G>A GRCh38
NC_000001.10:g.15772272G>A , CM000663.1:g.15772272G>A GRCh37
NC_000001.9:g.15644859G>A NCBI36
NG_009253.1:g.12335G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+28G>A MANE Select ENSP00000365116.4:n.792+28G>A
ENST00000375943.6:c.*246+28G>A ENSP00000365110.2:n.*246+28G>A
ENST00000375949.4:c.792+28G>A ENSP00000365116.4:n.792+28G>A
ENST00000483406.1:n.556+28G>A
NM_007272.2:c.792+28G>A NP_009203.2:n.792+28G>A
XM_011540550.1:c.646+28G>A XP_011538852.1:n.646+28G>A
NM_007272.3:c.792+28G>A MANE Select NP_009203.2:n.792+28G>A
Search 100 bp 5'
Search 100 bp 3'