Canonical Allele Identifier: CA1726783428
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426585A= , CM000669.2:g.94426585A= GRCh38
NC_000007.13:g.94055897A= , CM000669.1:g.94055897A= GRCh37
NC_000007.12:g.93893833A= NCBI36
NG_007405.1:g.37025A= , LRG_2:g.37025A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.3105+55A= MANE Select ENSP00000297268.6:n.3105+55A=
ENST00000297268.10:c.3105+55A= ENSP00000297268.6:n.3105+55A=
ENST00000478215.1:n.719A=
ENST00000481570.5:n.3133A=
ENST00000488121.1:n.21+55A=
ENST00000620463.1:c.3099+55A= ENSP00000477719.1:n.3099+55A=
NM_000089.3:c.3105+55A= , LRG_2t1:c.3105+55A= NP_000080.2:n.3105+55A=
NM_000089.4:c.3105+55A= MANE Select NP_000080.2:n.3105+55A=