Canonical Allele Identifier: CA62594649
Gene: COL3A1 HGNC NCBI

Linked Data

dbSNP Id: rs771300189
MyVariant Identifiers: chr2:g.189858196T>G (hg19) chr2:g.188993470T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188993470T>G , CM000664.2:g.188993470T>G GRCh38
NC_000002.11:g.189858196T>G , CM000664.1:g.189858196T>G GRCh37
NC_000002.10:g.189566441T>G NCBI36
NG_007404.1:g.24098T>G , LRG_3:g.24098T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000450867.2:c.1050+530T>G ENSP00000415346.2:n.1050+530T>G
ENST00000304636.9:c.1149+11T>G MANE Select ENSP00000304408.4:n.1149+11T>G
ENST00000304636.7:c.1149+11T>G ENSP00000304408.3:n.1149+11T>G
ENST00000317840.9:c.1149+11T>G ENSP00000315243.6:n.1149+11T>G
ENST00000450867.1:c.148+530T>G
NM_000090.3:c.1149+11T>G , LRG_3t1:c.1149+11T>G NP_000081.1:n.1149+11T>G
NM_000090.4:c.1149+11T>G MANE Select NP_000081.2:n.1149+11T>G
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