Canonical Allele Identifier: CA8645449

Gene: COL1A1

Linked Data

• dbSNP Id: rs376795563
• ExAC: 17:48273490 C / G
• gnomAD v2: 17-48273490-C-G
• gnomAD v3: 17-50196129-C-G
• gnomAD v4: 17-50196129-C-G
• MyVariant Identifiers: chr17:g.48273490C>G (hg19) ; chr17:g.50196129C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50196129C>G , CM000679.2:g.50196129C>G	GRCh38
NC_000017.10:g.48273490C>G , CM000679.1:g.48273490C>G	GRCh37
NC_000017.9:g.45628489C>G	NCBI36
NG_007400.1:g.10511G>C , LRG_1:g.10511G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1002+26G>C MANE Select	ENSP00000225964.6:n.1002+26G>C
ENST00000225964.9:c.1002+26G>C	ENSP00000225964.5:n.1002+26G>C
ENST00000485870.1:n.353G>C
NM_000088.3:c.1002+26G>C , LRG_1t1:c.1002+26G>C	NP_000079.2:n.1002+26G>C
XM_005257058.3:c.1002+26G>C	XP_005257115.2:n.1002+26G>C
XM_005257059.3:c.957+185G>C	XP_005257116.2:n.957+185G>C
XM_011524341.1:c.957+185G>C	XP_011522643.1:n.957+185G>C
XM_005257058.4:c.1002+26G>C	XP_005257115.2:n.1002+26G>C
XM_005257059.4:c.957+185G>C	XP_005257116.2:n.957+185G>C
NM_000088.4:c.1002+26G>C MANE Select	NP_000079.2:n.1002+26G>C