Canonical Allele Identifier: CA291546971

Gene: COL1A1

Linked Data

• dbSNP Id: rs958399216
• gnomAD v3: 17-50195844-C-A
• gnomAD v4: 17-50195844-C-A
• MyVariant Identifiers: chr17:g.48273205C>A (hg19) ; chr17:g.50195844C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50195844C>A , CM000679.2:g.50195844C>A	GRCh38
NC_000017.10:g.48273205C>A , CM000679.1:g.48273205C>A	GRCh37
NC_000017.9:g.45628204C>A	NCBI36
NG_007400.1:g.10796G>T , LRG_1:g.10796G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000225964.10:c.1056+79G>T MANE Select	ENSP00000225964.6:n.1056+79G>T
ENST00000225964.9:c.1056+79G>T	ENSP00000225964.5:n.1056+79G>T
NM_000088.3:c.1056+79G>T , LRG_1t1:c.1056+79G>T	NP_000079.2:n.1056+79G>T
XM_005257058.3:c.1056+79G>T	XP_005257115.2:n.1056+79G>T
XM_005257059.3:c.957+470G>T	XP_005257116.2:n.957+470G>T
XM_011524341.1:c.958-366G>T	XP_011522643.1:n.958-366G>T
XM_005257058.4:c.1056+79G>T	XP_005257115.2:n.1056+79G>T
XM_005257059.4:c.957+470G>T	XP_005257116.2:n.957+470G>T
NM_000088.4:c.1056+79G>T MANE Select	NP_000079.2:n.1056+79G>T