Canonical Allele Identifier: CA1155328463
Gene: CTRC HGNC NCBI

Linked Data

dbSNP Id: rs1708203817

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.643dup
ENST00000375943.6:c.*97dup
ENST00000375949.4:c.643dup
ENST00000483406.1:n.407dup
NM_007272.2:c.643dup
XM_011540550.1:c.497dup
NM_007272.3:c.643dup