Canonical Allele Identifier: CA338567675
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15772095G>C (hg19) chr1:g.15445600G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445600G>C , CM000663.2:g.15445600G>C GRCh38
NC_000001.10:g.15772095G>C , CM000663.1:g.15772095G>C GRCh37
NC_000001.9:g.15644682G>C NCBI36
NG_009253.1:g.12158G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.643G>C MANE Select ENSP00000365116.4:p.Asp215His
ENST00000375943.6:c.*97G>C ENSP00000365110.2:n.*97G>C
ENST00000375949.4:c.643G>C ENSP00000365116.4:p.Asp215His
ENST00000483406.1:n.407G>C
NM_007272.2:c.643G>C NP_009203.2:p.Asp215His
XM_011540550.1:c.497G>C XP_011538852.1:p.Gly166Ala
NM_007272.3:c.643G>C MANE Select NP_009203.2:p.Asp215His
Search 100 bp 5'
Search 100 bp 3'