Canonical Allele Identifier: CA291543350

Gene: COL1A1

Linked Data

• dbSNP Id: rs200581751
• gnomAD v3: 17-50190293-G-C
• gnomAD v4: 17-50190293-G-C
• MyVariant Identifiers: chr17:g.48267654G>C (hg19) ; chr17:g.50190293G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50190293G>C , CM000679.2:g.50190293G>C	GRCh38
NC_000017.10:g.48267654G>C , CM000679.1:g.48267654G>C	GRCh37
NC_000017.9:g.45622653G>C	NCBI36
NG_007400.1:g.16347C>G , LRG_1:g.16347C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.2451+34C>G MANE Select	ENSP00000225964.6:n.2451+34C>G
ENST00000225964.9:c.2451+34C>G	ENSP00000225964.5:n.2451+34C>G
NM_000088.3:c.2451+34C>G , LRG_1t1:c.2451+34C>G	NP_000079.2:n.2451+34C>G
XM_005257058.3:c.2451+34C>G	XP_005257115.2:n.2451+34C>G
XM_005257059.3:c.1533+34C>G	XP_005257116.2:n.1533+34C>G
XM_011524341.1:c.2253+34C>G	XP_011522643.1:n.2253+34C>G
XM_005257058.4:c.2451+34C>G	XP_005257115.2:n.2451+34C>G
XM_005257059.4:c.1533+34C>G	XP_005257116.2:n.1533+34C>G
NM_000088.4:c.2451+34C>G MANE Select	NP_000079.2:n.2451+34C>G