Canonical Allele Identifier: CA613428
Gene: CTRC HGNC NCBI

Linked Data

dbSNP Id: rs769089707
ExAC: 1:15772070 A / G
gnomAD v2: 1-15772070-A-G
gnomAD v4: 1-15445575-A-G
MyVariant Identifiers: chr1:g.15772070A>G (hg19) chr1:g.15445575A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445575A>G , CM000663.2:g.15445575A>G GRCh38
NC_000001.10:g.15772070A>G , CM000663.1:g.15772070A>G GRCh37
NC_000001.9:g.15644657A>G NCBI36
NG_009253.1:g.12133A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.640-22A>G MANE Select ENSP00000365116.4:n.640-22A>G
ENST00000375943.6:c.*94-22A>G ENSP00000365110.2:n.*94-22A>G
ENST00000375949.4:c.640-22A>G ENSP00000365116.4:n.640-22A>G
ENST00000483406.1:n.404-22A>G
NM_007272.2:c.640-22A>G NP_009203.2:n.640-22A>G
XM_011540550.1:c.494-22A>G XP_011538852.1:n.494-22A>G
NM_007272.3:c.640-22A>G MANE Select NP_009203.2:n.640-22A>G
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