Canonical Allele Identifier: CA1726792241
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404795A= , CM000669.2:g.94404795A= GRCh38
NC_000007.13:g.94034107A= , CM000669.1:g.94034107A= GRCh37
NC_000007.12:g.93872043A= NCBI36
NG_007405.1:g.15235A= , LRG_2:g.15235A=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.379-44A= MANE Select ENSP00000297268.6:n.379-44A=
ENST00000297268.10:c.379-44A= ENSP00000297268.6:n.379-44A=
ENST00000620463.1:c.373-44A= ENSP00000477719.1:n.373-44A=
NM_000089.3:c.379-44A= , LRG_2t1:c.379-44A= NP_000080.2:n.379-44A=
NM_000089.4:c.379-44A= MANE Select NP_000080.2:n.379-44A=