Canonical Allele Identifier: CA430313141
Gene: COL3A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189871698T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189006972T>G , CM000664.2:g.189006972T>G GRCh38
NC_000002.11:g.189871698T>G , CM000664.1:g.189871698T>G GRCh37
NC_000002.10:g.189579943T>G NCBI36
NG_007404.1:g.37600T>G , LRG_3:g.37600T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.3138T>G ENSP00000415346.2:p.Ala1046=
ENST00000304636.9:c.3237T>G MANE Select ENSP00000304408.4:p.Ala1079=
ENST00000304636.7:c.3237T>G ENSP00000304408.3:p.Ala1079=
ENST00000317840.9:c.2528-1082T>G ENSP00000315243.6:n.2528-1082T>G
NM_000090.3:c.3237T>G , LRG_3t1:c.3237T>G NP_000081.1:p.Ala1079=
NM_000090.4:c.3237T>G MANE Select NP_000081.2:p.Ala1079=
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