Canonical Allele Identifier: CA347179574

Gene: CD207

Linked Data

• dbSNP Id: rs527591997
• MyVariant Identifiers: chr2:g.71058931G>C (hg19) ; chr2:g.70831800G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831800G>C , CM000664.2:g.70831800G>C	GRCh38
NC_000002.11:g.71058931G>C , CM000664.1:g.71058931G>C	GRCh37
NC_000002.10:g.70912439G>C	NCBI36
NG_033914.1:g.9024C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.737C>G MANE Select	ENSP00000386378.3:p.Ala246Gly
ENST00000410009.4:c.737C>G	ENSP00000386378.3:p.Ala246Gly
NM_015717.4:c.737C>G	NP_056532.4:p.Ala246Gly
XM_011532874.1:c.737C>G	XP_011531176.1:p.Ala246Gly
XM_011532875.1:c.737C>G	XP_011531177.1:p.Ala246Gly
XM_011532876.1:c.737C>G	XP_011531178.1:p.Ala246Gly
XM_011532875.2:c.737C>G	XP_011531177.1:p.Ala246Gly
XM_011532876.2:c.737C>G	XP_011531178.1:p.Ala246Gly
NM_015717.5:c.737C>G MANE Select	NP_056532.4:p.Ala246Gly