Canonical Allele Identifier: CA626689040

Gene: COL1A1

Linked Data

• dbSNP Id: rs768460126
• gnomAD v2: 17-48263041-A-G
• gnomAD v4: 17-50185680-A-G
• MyVariant Identifiers: chr17:g.48263041A>G (hg19) ; chr17:g.50185680A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185680A>G , CM000679.2:g.50185680A>G	GRCh38
NC_000017.10:g.48263041A>G , CM000679.1:g.48263041A>G	GRCh37
NC_000017.9:g.45618040A>G	NCBI36
NG_007400.1:g.20960T>C , LRG_1:g.20960T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4249-32T>C MANE Select	ENSP00000225964.6:n.4249-32T>C
ENST00000225964.9:c.4249-32T>C	ENSP00000225964.5:n.4249-32T>C
NM_000088.3:c.4249-32T>C , LRG_1t1:c.4249-32T>C	NP_000079.2:n.4249-32T>C
XM_005257058.3:c.3979-32T>C	XP_005257115.2:n.3979-32T>C
XM_005257059.3:c.3331-32T>C	XP_005257116.2:n.3331-32T>C
XM_011524341.1:c.4051-32T>C	XP_011522643.1:n.4051-32T>C
XM_005257058.4:c.3979-32T>C	XP_005257115.2:n.3979-32T>C
XM_005257059.4:c.3331-32T>C	XP_005257116.2:n.3331-32T>C
NM_000088.4:c.4249-32T>C MANE Select	NP_000079.2:n.4249-32T>C