Canonical Allele Identifier: CA500844377
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48265897A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188536A>G , CM000679.2:g.50188536A>G GRCh38
NC_000017.10:g.48265897A>G , CM000679.1:g.48265897A>G GRCh37
NC_000017.9:g.45620896A>G NCBI36
NG_007400.1:g.18104T>C , LRG_1:g.18104T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.3201T>C MANE Select ENSP00000225964.6:p.Gly1067=
ENST00000225964.9:c.3201T>C ENSP00000225964.5:p.Gly1067=
ENST00000486572.1:n.19T>C
ENST00000511732.1:n.145T>C
NM_000088.3:c.3201T>C , LRG_1t1:c.3201T>C NP_000079.2:p.Gly1067=
XM_005257058.3:c.2931T>C XP_005257115.2:p.Gly977=
XM_005257059.3:c.2283T>C XP_005257116.2:p.Gly761=
XM_011524341.1:c.3003T>C XP_011522643.1:p.Gly1001=
XM_005257058.4:c.2931T>C XP_005257115.2:p.Gly977=
XM_005257059.4:c.2283T>C XP_005257116.2:p.Gly761=
NM_000088.4:c.3201T>C MANE Select NP_000079.2:p.Gly1067=