Canonical Allele Identifier: CA338565019
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15767025C>G (hg19) chr1:g.15440529C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15440529C>G , CM000663.2:g.15440529C>G GRCh38
NC_000001.10:g.15767025C>G , CM000663.1:g.15767025C>G GRCh37
NC_000001.9:g.15639612C>G NCBI36
NG_009253.1:g.7088C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.169C>G MANE Select ENSP00000365116.4:p.His57Asp
ENST00000375943.6:c.41-1918C>G ENSP00000365110.2:n.41-1918C>G
ENST00000375949.4:c.169C>G ENSP00000365116.4:p.His57Asp
ENST00000476813.5:n.53-1918C>G
ENST00000483406.1:n.79C>G
NM_007272.2:c.169C>G NP_009203.2:p.His57Asp
XM_011540550.1:c.169C>G XP_011538852.1:p.His57Asp
NM_007272.3:c.169C>G MANE Select NP_009203.2:p.His57Asp
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