Canonical Allele Identifier: CA1726793773
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94408214G= , CM000669.2:g.94408214G= GRCh38
NC_000007.13:g.94037526G= , CM000669.1:g.94037526G= GRCh37
NC_000007.12:g.93875462G= NCBI36
NG_007405.1:g.18654G= , LRG_2:g.18654G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.671G= MANE Select ENSP00000297268.6:p.Arg224=
ENST00000297268.10:c.671G= ENSP00000297268.6:p.Arg224=
ENST00000620463.1:c.665G= ENSP00000477719.1:p.Arg222=
NM_000089.3:c.671G= , LRG_2t1:c.671G= NP_000080.2:p.Arg224=
NM_000089.4:c.671G= MANE Select NP_000080.2:p.Arg224=