Canonical Allele Identifier: CA2578942240
Gene: COL1A2 HGNC NCBI

Linked Data

gnomAD v4: 7-94426561-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426561A>C , CM000669.2:g.94426561A>C GRCh38
NC_000007.13:g.94055873A>C , CM000669.1:g.94055873A>C GRCh37
NC_000007.12:g.93893809A>C NCBI36
NG_007405.1:g.37001A>C , LRG_2:g.37001A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.3105+31A>C MANE Select ENSP00000297268.6:n.3105+31A>C
ENST00000297268.10:c.3105+31A>C ENSP00000297268.6:n.3105+31A>C
ENST00000478215.1:n.695A>C
ENST00000481570.5:n.3109A>C
ENST00000488121.1:n.21+31A>C
ENST00000620463.1:c.3099+31A>C ENSP00000477719.1:n.3099+31A>C
NM_000089.3:c.3105+31A>C , LRG_2t1:c.3105+31A>C NP_000080.2:n.3105+31A>C
NM_000089.4:c.3105+31A>C MANE Select NP_000080.2:n.3105+31A>C