Canonical Allele Identifier: CA49670220

Gene: CD207

Linked Data

• dbSNP Id: rs782255038
• gnomAD v4: 2-70831833-A-G
• MyVariant Identifiers: chr2:g.71058964A>G (hg19) ; chr2:g.70831833A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831833A>G , CM000664.2:g.70831833A>G	GRCh38
NC_000002.11:g.71058964A>G , CM000664.1:g.71058964A>G	GRCh37
NC_000002.10:g.70912472A>G	NCBI36
NG_033914.1:g.8991T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.718-14T>C MANE Select	ENSP00000386378.3:n.718-14T>C
ENST00000410009.4:c.718-14T>C	ENSP00000386378.3:n.718-14T>C
NM_015717.4:c.718-14T>C	NP_056532.4:n.718-14T>C
XM_011532874.1:c.718-14T>C	XP_011531176.1:n.718-14T>C
XM_011532875.1:c.718-14T>C	XP_011531177.1:n.718-14T>C
XM_011532876.1:c.718-14T>C	XP_011531178.1:n.718-14T>C
XM_011532875.2:c.718-14T>C	XP_011531177.1:n.718-14T>C
XM_011532876.2:c.718-14T>C	XP_011531178.1:n.718-14T>C
NM_015717.5:c.718-14T>C MANE Select	NP_056532.4:n.718-14T>C