Canonical Allele Identifier: CA1726767661
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94417802G= , CM000669.2:g.94417802G= GRCh38
NC_000007.13:g.94047114G= , CM000669.1:g.94047114G= GRCh37
NC_000007.12:g.93885050G= NCBI36
NG_007405.1:g.28242G= , LRG_2:g.28242G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.1942G= MANE Select ENSP00000297268.6:p.Ala648=
ENST00000297268.10:c.1942G= ENSP00000297268.6:p.Ala648=
ENST00000461525.5:n.31G=
ENST00000473573.5:n.279G=
ENST00000497316.5:n.339G=
ENST00000620463.1:c.1936G= ENSP00000477719.1:p.Ala646=
NM_000089.3:c.1942G= , LRG_2t1:c.1942G= NP_000080.2:p.Ala648=
NM_000089.4:c.1942G= MANE Select NP_000080.2:p.Ala648=