Canonical Allele Identifier: CA2733837655
Gene: COL1A1 HGNC NCBI

Linked Data

dbSNP Id: rs2144570619

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194249A>G , CM000679.2:g.50194249A>G GRCh38
NC_000017.10:g.48271610A>G , CM000679.1:g.48271610A>G GRCh37
NC_000017.9:g.45626609A>G NCBI36
NG_007400.1:g.12391T>C , LRG_1:g.12391T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1615-66T>C MANE Select ENSP00000225964.6:n.1615-66T>C
ENST00000225964.9:c.1615-66T>C ENSP00000225964.5:n.1615-66T>C
ENST00000463440.1:n.5-66T>C
ENST00000471344.1:n.559-66T>C
NM_000088.3:c.1615-66T>C , LRG_1t1:c.1615-66T>C NP_000079.2:n.1615-66T>C
XM_005257058.3:c.1615-66T>C XP_005257115.2:n.1615-66T>C
XM_005257059.3:c.958-1556T>C XP_005257116.2:n.958-1556T>C
XM_011524341.1:c.1417-66T>C XP_011522643.1:n.1417-66T>C
XM_005257058.4:c.1615-66T>C XP_005257115.2:n.1615-66T>C
XM_005257059.4:c.958-1556T>C XP_005257116.2:n.958-1556T>C
NM_000088.4:c.1615-66T>C MANE Select NP_000079.2:n.1615-66T>C