Canonical Allele Identifier: CA1726783467
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426605A= , CM000669.2:g.94426605A= GRCh38
NC_000007.13:g.94055917A= , CM000669.1:g.94055917A= GRCh37
NC_000007.12:g.93893853A= NCBI36
NG_007405.1:g.37045A= , LRG_2:g.37045A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.3105+75A= MANE Select ENSP00000297268.6:n.3105+75A=
ENST00000297268.10:c.3105+75A= ENSP00000297268.6:n.3105+75A=
ENST00000478215.1:n.739A=
ENST00000481570.5:n.3153A=
ENST00000488121.1:n.21+75A=
ENST00000620463.1:c.3099+75A= ENSP00000477719.1:n.3099+75A=
NM_000089.3:c.3105+75A= , LRG_2t1:c.3105+75A= NP_000080.2:n.3105+75A=
NM_000089.4:c.3105+75A= MANE Select NP_000080.2:n.3105+75A=