Canonical Allele Identifier: CA4346642
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs763980453
ExAC: 7:94034084 A / G
gnomAD v2: 7-94034084-A-G
gnomAD v3: 7-94404772-A-G
gnomAD v4: 7-94404772-A-G
MyVariant Identifiers: chr7:g.94034084A>G (hg19) chr7:g.94404772A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404772A>G , CM000669.2:g.94404772A>G GRCh38
NC_000007.13:g.94034084A>G , CM000669.1:g.94034084A>G GRCh37
NC_000007.12:g.93872020A>G NCBI36
NG_007405.1:g.15212A>G , LRG_2:g.15212A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.378+26A>G MANE Select ENSP00000297268.6:n.378+26A>G
ENST00000297268.10:c.378+26A>G ENSP00000297268.6:n.378+26A>G
ENST00000620463.1:c.372+26A>G ENSP00000477719.1:n.372+26A>G
NM_000089.3:c.378+26A>G , LRG_2t1:c.378+26A>G NP_000080.2:n.378+26A>G
NM_000089.4:c.378+26A>G MANE Select NP_000080.2:n.378+26A>G
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