Canonical Allele Identifier: CA2263918315
Gene: COL1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1907409083

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194668G>T , CM000679.2:g.50194668G>T GRCh38
NC_000017.10:g.48272029G>T , CM000679.1:g.48272029G>T GRCh37
NC_000017.9:g.45627028G>T NCBI36
NG_007400.1:g.11972C>A , LRG_1:g.11972C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1462-42C>A MANE Select ENSP00000225964.6:n.1462-42C>A
ENST00000225964.9:c.1462-42C>A ENSP00000225964.5:n.1462-42C>A
ENST00000471344.1:n.406-42C>A
NM_000088.3:c.1462-42C>A , LRG_1t1:c.1462-42C>A NP_000079.2:n.1462-42C>A
XM_005257058.3:c.1462-42C>A XP_005257115.2:n.1462-42C>A
XM_005257059.3:c.957+1646C>A XP_005257116.2:n.957+1646C>A
XM_011524341.1:c.1264-42C>A XP_011522643.1:n.1264-42C>A
XM_005257058.4:c.1462-42C>A XP_005257115.2:n.1462-42C>A
XM_005257059.4:c.957+1646C>A XP_005257116.2:n.957+1646C>A
NM_000088.4:c.1462-42C>A MANE Select NP_000079.2:n.1462-42C>A