Canonical Allele Identifier: CA49670164

Gene: CD207

Linked Data

• dbSNP Id: rs781817790
• gnomAD v4: 2-70831675-T-G
• MyVariant Identifiers: chr2:g.71058806T>G (hg19) ; chr2:g.70831675T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831675T>G , CM000664.2:g.70831675T>G	GRCh38
NC_000002.11:g.71058806T>G , CM000664.1:g.71058806T>G	GRCh37
NC_000002.10:g.70912314T>G	NCBI36
NG_033914.1:g.9149A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.836+26A>C MANE Select	ENSP00000386378.3:n.836+26A>C
ENST00000410009.4:c.836+26A>C	ENSP00000386378.3:n.836+26A>C
NM_015717.4:c.836+26A>C	NP_056532.4:n.836+26A>C
XM_011532874.1:c.836+26A>C	XP_011531176.1:n.836+26A>C
XM_011532875.1:c.836+26A>C	XP_011531177.1:n.836+26A>C
XM_011532876.1:c.836+26A>C	XP_011531178.1:n.836+26A>C
XM_011532875.2:c.836+26A>C	XP_011531177.1:n.836+26A>C
XM_011532876.2:c.836+26A>C	XP_011531178.1:n.836+26A>C
NM_015717.5:c.836+26A>C MANE Select	NP_056532.4:n.836+26A>C