Canonical Allele Identifier: CA1104599366
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1792282267
gnomAD v3: 7-94426585-A-T
gnomAD v4: 7-94426585-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426585A>T , CM000669.2:g.94426585A>T GRCh38
NC_000007.13:g.94055897A>T , CM000669.1:g.94055897A>T GRCh37
NC_000007.12:g.93893833A>T NCBI36
NG_007405.1:g.37025A>T , LRG_2:g.37025A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.3105+55A>T MANE Select ENSP00000297268.6:n.3105+55A>T
ENST00000297268.10:c.3105+55A>T ENSP00000297268.6:n.3105+55A>T
ENST00000478215.1:n.719A>T
ENST00000481570.5:n.3133A>T
ENST00000488121.1:n.21+55A>T
ENST00000620463.1:c.3099+55A>T ENSP00000477719.1:n.3099+55A>T
NM_000089.3:c.3105+55A>T , LRG_2t1:c.3105+55A>T NP_000080.2:n.3105+55A>T
NM_000089.4:c.3105+55A>T MANE Select NP_000080.2:n.3105+55A>T
Search 100 bp 5'
Search 100 bp 3'