Canonical Allele Identifier: CA1726781641
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94425657A= , CM000669.2:g.94425657A= GRCh38
NC_000007.13:g.94054969A= , CM000669.1:g.94054969A= GRCh37
NC_000007.12:g.93892905A= NCBI36
NG_007405.1:g.36097A= , LRG_2:g.36097A=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2829A= MANE Select ENSP00000297268.6:p.Gly943=
ENST00000297268.10:c.2829A= ENSP00000297268.6:p.Gly943=
ENST00000469732.1:n.612A=
ENST00000478215.1:n.388A=
ENST00000481570.5:n.2802A=
ENST00000620463.1:c.2823A= ENSP00000477719.1:p.Gly941=
NM_000089.3:c.2829A= , LRG_2t1:c.2829A= NP_000080.2:p.Gly943=
NM_000089.4:c.2829A= MANE Select NP_000080.2:p.Gly943=