Canonical Allele Identifier: CA368219724
Gene: COL1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94034193G>C (hg19) chr7:g.94404881G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404881G>C , CM000669.2:g.94404881G>C GRCh38
NC_000007.13:g.94034193G>C , CM000669.1:g.94034193G>C GRCh37
NC_000007.12:g.93872129G>C NCBI36
NG_007405.1:g.15321G>C , LRG_2:g.15321G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.421G>C MANE Select ENSP00000297268.6:p.Ala141Pro
ENST00000297268.10:c.421G>C ENSP00000297268.6:p.Ala141Pro
ENST00000620463.1:c.415G>C ENSP00000477719.1:p.Ala139Pro
NM_000089.3:c.421G>C , LRG_2t1:c.421G>C NP_000080.2:p.Ala141Pro
NM_000089.4:c.421G>C MANE Select NP_000080.2:p.Ala141Pro
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