Canonical Allele Identifier: CA2659494997

Gene: CD207

Linked Data

• gnomAD v4: 2-70831939-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831939G>T , CM000664.2:g.70831939G>T	GRCh38
NC_000002.11:g.71059070G>T , CM000664.1:g.71059070G>T	GRCh37
NC_000002.10:g.70912578G>T	NCBI36
NG_033914.1:g.8885C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.718-120C>A MANE Select	ENSP00000386378.3:n.718-120C>A
ENST00000410009.4:c.718-120C>A	ENSP00000386378.3:n.718-120C>A
NM_015717.4:c.718-120C>A	NP_056532.4:n.718-120C>A
XM_011532874.1:c.718-120C>A	XP_011531176.1:n.718-120C>A
XM_011532875.1:c.718-120C>A	XP_011531177.1:n.718-120C>A
XM_011532876.1:c.718-120C>A	XP_011531178.1:n.718-120C>A
XM_011532875.2:c.718-120C>A	XP_011531177.1:n.718-120C>A
XM_011532876.2:c.718-120C>A	XP_011531178.1:n.718-120C>A
NM_015717.5:c.718-120C>A MANE Select	NP_056532.4:n.718-120C>A