Canonical Allele Identifier: CA843998536
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1377458801

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404635A>C , CM000669.2:g.94404635A>C GRCh38
NC_000007.13:g.94033947A>C , CM000669.1:g.94033947A>C GRCh37
NC_000007.12:g.93871883A>C NCBI36
NG_007405.1:g.15075A>C , LRG_2:g.15075A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.324+35A>C MANE Select ENSP00000297268.6:n.324+35A>C
ENST00000297268.10:c.324+35A>C ENSP00000297268.6:n.324+35A>C
ENST00000620463.1:c.318+35A>C ENSP00000477719.1:n.318+35A>C
NM_000089.3:c.324+35A>C , LRG_2t1:c.324+35A>C NP_000080.2:n.324+35A>C
NM_000089.4:c.324+35A>C MANE Select NP_000080.2:n.324+35A>C