Canonical Allele Identifier: CA1726767754
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94417808A= , CM000669.2:g.94417808A= GRCh38
NC_000007.13:g.94047120A= , CM000669.1:g.94047120A= GRCh37
NC_000007.12:g.93885056A= NCBI36
NG_007405.1:g.28248A= , LRG_2:g.28248A=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.1948A= MANE Select ENSP00000297268.6:p.Ile650=
ENST00000297268.10:c.1948A= ENSP00000297268.6:p.Ile650=
ENST00000461525.5:n.37A=
ENST00000473573.5:n.285A=
ENST00000497316.5:n.345A=
ENST00000620463.1:c.1942A= ENSP00000477719.1:p.Ile648=
NM_000089.3:c.1948A= , LRG_2t1:c.1948A= NP_000080.2:p.Ile650=
NM_000089.4:c.1948A= MANE Select NP_000080.2:p.Ile650=