Canonical Allele Identifier: CA2683769683
Gene: COL1A2 HGNC NCBI

Linked Data

gnomAD v4: 7-94415276-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94415276T>G , CM000669.2:g.94415276T>G GRCh38
NC_000007.13:g.94044588T>G , CM000669.1:g.94044588T>G GRCh37
NC_000007.12:g.93882524T>G NCBI36
NG_007405.1:g.25716T>G , LRG_2:g.25716T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.1764+6T>G MANE Select ENSP00000297268.6:n.1764+6T>G
ENST00000297268.10:c.1764+6T>G ENSP00000297268.6:n.1764+6T>G
ENST00000473573.5:n.101+6T>G
ENST00000488298.5:n.188+6T>G
ENST00000620463.1:c.1758+6T>G ENSP00000477719.1:n.1758+6T>G
NM_000089.3:c.1764+6T>G , LRG_2t1:c.1764+6T>G NP_000080.2:n.1764+6T>G
NM_000089.4:c.1764+6T>G MANE Select NP_000080.2:n.1764+6T>G
Search 100 bp 5'
Search 100 bp 3'