Canonical Allele Identifier: CA2378212

Gene: COL7A1

Linked Data

• ClinVar Variation Id: 2790503
• ClinVar RCV Id: RCV003669919
• dbSNP Id: rs759938995
• ExAC: 3:48605083 G / A
• gnomAD v2: 3-48605083-G-A
• gnomAD v4: 3-48567650-G-A
• MyVariant Identifiers: chr3:g.48605083G>A (hg19) ; chr3:g.48567650G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48567650G>A , CM000665.2:g.48567650G>A	GRCh38
NC_000003.11:g.48605083G>A , CM000665.1:g.48605083G>A	GRCh37
NC_000003.10:g.48580087G>A	NCBI36
NG_007065.1:g.32603C>T , LRG_286:g.32603C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7984-14C>T MANE Select	ENSP00000506558.1:n.7984-14C>T
ENST00000328333.12:c.7984-14C>T	ENSP00000332371.8:n.7984-14C>T
ENST00000487017.5:n.4623-14C>T
NM_000094.3:c.7984-14C>T , LRG_286t1:c.7984-14C>T	NP_000085.1:n.7984-14C>T
XM_011533336.1:c.8011-14C>T	XP_011531638.1:n.8011-14C>T
XM_011533337.1:c.7984-14C>T	XP_011531639.1:n.7984-14C>T
XM_011533338.1:c.7951-14C>T	XP_011531640.1:n.7951-14C>T
XR_940369.1:n.8047-14C>T
XR_940370.1:n.8047-14C>T
XR_940371.1:n.8047-14C>T
XM_017005688.1:c.7924-14C>T	XP_016861177.1:n.7924-14C>T
XR_001740003.1:n.8020-14C>T
XR_001740004.1:n.8020-14C>T
XR_001740005.1:n.8020-14C>T
NM_000094.4:c.7984-14C>T MANE Select	NP_000085.1:n.7984-14C>T