Canonical Allele Identifier: CA1726790722
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94401208T= , CM000669.2:g.94401208T= GRCh38
NC_000007.13:g.94030520T= , CM000669.1:g.94030520T= GRCh37
NC_000007.12:g.93868456T= NCBI36
NG_007405.1:g.11648T= , LRG_2:g.11648T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.226-359T= MANE Select ENSP00000297268.6:n.226-359T=
ENST00000297268.10:c.226-359T= ENSP00000297268.6:n.226-359T=
ENST00000620463.1:c.220-359T= ENSP00000477719.1:n.220-359T=
NM_000089.3:c.226-359T= , LRG_2t1:c.226-359T= NP_000080.2:n.226-359T=
NM_000089.4:c.226-359T= MANE Select NP_000080.2:n.226-359T=