Canonical Allele Identifier: CA500847879
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48270019A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192658A>C , CM000679.2:g.50192658A>C GRCh38
NC_000017.10:g.48270019A>C , CM000679.1:g.48270019A>C GRCh37
NC_000017.9:g.45625018A>C NCBI36
NG_007400.1:g.13982T>G , LRG_1:g.13982T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1911T>G MANE Select ENSP00000225964.6:p.Ala637=
ENST00000225964.9:c.1911T>G ENSP00000225964.5:p.Ala637=
ENST00000476387.1:n.260T>G
NM_000088.3:c.1911T>G , LRG_1t1:c.1911T>G NP_000079.2:p.Ala637=
XM_005257058.3:c.1911T>G XP_005257115.2:p.Ala637=
XM_005257059.3:c.993T>G XP_005257116.2:p.Ala331=
XM_011524341.1:c.1713T>G XP_011522643.1:p.Ala571=
XM_005257058.4:c.1911T>G XP_005257115.2:p.Ala637=
XM_005257059.4:c.993T>G XP_005257116.2:p.Ala331=
NM_000088.4:c.1911T>G MANE Select NP_000079.2:p.Ala637=