Canonical Allele Identifier: CA1726790952
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94401696A= , CM000669.2:g.94401696A= GRCh38
NC_000007.13:g.94031008A= , CM000669.1:g.94031008A= GRCh37
NC_000007.12:g.93868944A= NCBI36
NG_007405.1:g.12136A= , LRG_2:g.12136A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.279+76A= MANE Select ENSP00000297268.6:n.279+76A=
ENST00000297268.10:c.279+76A= ENSP00000297268.6:n.279+76A=
ENST00000620463.1:c.273+76A= ENSP00000477719.1:n.273+76A=
NM_000089.3:c.279+76A= , LRG_2t1:c.279+76A= NP_000080.2:n.279+76A=
NM_000089.4:c.279+76A= MANE Select NP_000080.2:n.279+76A=