Canonical Allele Identifier: CA2263919618
Gene: COL1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1907665751

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50197136C>T , CM000679.2:g.50197136C>T GRCh38
NC_000017.10:g.48274497C>T , CM000679.1:g.48274497C>T GRCh37
NC_000017.9:g.45629496C>T NCBI36
NG_007400.1:g.9504G>A , LRG_1:g.9504G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.750+44G>A MANE Select ENSP00000225964.6:n.750+44G>A
ENST00000225964.9:c.750+44G>A ENSP00000225964.5:n.750+44G>A
ENST00000495677.1:n.477+44G>A
NM_000088.3:c.750+44G>A , LRG_1t1:c.750+44G>A NP_000079.2:n.750+44G>A
XM_005257058.3:c.750+44G>A XP_005257115.2:n.750+44G>A
XM_005257059.3:c.750+44G>A XP_005257116.2:n.750+44G>A
XM_011524341.1:c.750+44G>A XP_011522643.1:n.750+44G>A
XM_005257058.4:c.750+44G>A XP_005257115.2:n.750+44G>A
XM_005257059.4:c.750+44G>A XP_005257116.2:n.750+44G>A
NM_000088.4:c.750+44G>A MANE Select NP_000079.2:n.750+44G>A