Canonical Allele Identifier: CA844001767
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1200868448
MyVariant Identifiers: chr7:g.94038507A>G (hg19) chr7:g.94409195A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409195A>G , CM000669.2:g.94409195A>G GRCh38
NC_000007.13:g.94038507A>G , CM000669.1:g.94038507A>G GRCh37
NC_000007.12:g.93876443A>G NCBI36
NG_007405.1:g.19635A>G , LRG_2:g.19635A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.793-127A>G MANE Select ENSP00000297268.6:n.793-127A>G
ENST00000297268.10:c.793-127A>G ENSP00000297268.6:n.793-127A>G
ENST00000620463.1:c.787-127A>G ENSP00000477719.1:n.787-127A>G
NM_000089.3:c.793-127A>G , LRG_2t1:c.793-127A>G NP_000080.2:n.793-127A>G
NM_000089.4:c.793-127A>G MANE Select NP_000080.2:n.793-127A>G
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