Canonical Allele Identifier: CA430312839
Gene: COL3A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189871136T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189006410T>A , CM000664.2:g.189006410T>A GRCh38
NC_000002.11:g.189871136T>A , CM000664.1:g.189871136T>A GRCh37
NC_000002.10:g.189579381T>A NCBI36
NG_007404.1:g.37038T>A , LRG_3:g.37038T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000450867.2:c.3060T>A ENSP00000415346.2:p.Gly1020=
ENST00000304636.9:c.3159T>A MANE Select ENSP00000304408.4:p.Gly1053=
ENST00000304636.7:c.3159T>A ENSP00000304408.3:p.Gly1053=
ENST00000317840.9:c.2528-1644T>A ENSP00000315243.6:n.2528-1644T>A
NM_000090.3:c.3159T>A , LRG_3t1:c.3159T>A NP_000081.1:p.Gly1053=
NM_000090.4:c.3159T>A MANE Select NP_000081.2:p.Gly1053=