Canonical Allele Identifier: CA347179623

Gene: CD207

Linked Data

• gnomAD v4: 2-70831821-T-A
• MyVariant Identifiers: chr2:g.71058952T>A (hg19) ; chr2:g.70831821T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831821T>A , CM000664.2:g.70831821T>A	GRCh38
NC_000002.11:g.71058952T>A , CM000664.1:g.71058952T>A	GRCh37
NC_000002.10:g.70912460T>A	NCBI36
NG_033914.1:g.9003A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.718-2A>T MANE Select	ENSP00000386378.3:n.718-2A>T
ENST00000410009.4:c.718-2A>T	ENSP00000386378.3:n.718-2A>T
NM_015717.4:c.718-2A>T	NP_056532.4:n.718-2A>T
XM_011532874.1:c.718-2A>T	XP_011531176.1:n.718-2A>T
XM_011532875.1:c.718-2A>T	XP_011531177.1:n.718-2A>T
XM_011532876.1:c.718-2A>T	XP_011531178.1:n.718-2A>T
XM_011532875.2:c.718-2A>T	XP_011531177.1:n.718-2A>T
XM_011532876.2:c.718-2A>T	XP_011531178.1:n.718-2A>T
NM_015717.5:c.718-2A>T MANE Select	NP_056532.4:n.718-2A>T