Canonical Allele Identifier: CA500844380
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48265900A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188539A>C , CM000679.2:g.50188539A>C GRCh38
NC_000017.10:g.48265900A>C , CM000679.1:g.48265900A>C GRCh37
NC_000017.9:g.45620899A>C NCBI36
NG_007400.1:g.18101T>G , LRG_1:g.18101T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.3198T>G MANE Select ENSP00000225964.6:p.Arg1066=
ENST00000225964.9:c.3198T>G ENSP00000225964.5:p.Arg1066=
ENST00000486572.1:n.16T>G
ENST00000511732.1:n.142T>G
NM_000088.3:c.3198T>G , LRG_1t1:c.3198T>G NP_000079.2:p.Arg1066=
XM_005257058.3:c.2928T>G XP_005257115.2:p.Arg976=
XM_005257059.3:c.2280T>G XP_005257116.2:p.Arg760=
XM_011524341.1:c.3000T>G XP_011522643.1:p.Arg1000=
XM_005257058.4:c.2928T>G XP_005257115.2:p.Arg976=
XM_005257059.4:c.2280T>G XP_005257116.2:p.Arg760=
NM_000088.4:c.3198T>G MANE Select NP_000079.2:p.Arg1066=