Canonical Allele Identifier: CA754961568

Gene: EDAR RANBP2

Linked Data

• dbSNP Id: rs1449090386
• MyVariant Identifiers: chr2:g.109524743T>C (hg19) ; chr2:g.108908287T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108908287T>C , CM000664.2:g.108908287T>C	GRCh38
NC_000002.11:g.109524743T>C , CM000664.1:g.109524743T>C	GRCh37
NC_000002.10:g.108891175T>C	NCBI36
NG_008257.1:g.86086A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.804-268A>G (EDAR) MANE Select	ENSP00000258443.2:n.804-268A>G
ENST00000258443.6:c.804-268A>G (EDAR)	ENSP00000258443.2:n.804-268A>G
ENST00000376651.1:c.900-268A>G (EDAR)	ENSP00000365839.1:n.900-268A>G
ENST00000409271.5:c.900-268A>G (EDAR)	ENSP00000386371.1:n.900-268A>G
NM_022336.3:c.804-268A>G (EDAR)	NP_071731.1:n.804-268A>G
XM_006712204.1:c.900-268A>G (EDAR)	XP_006712267.1:n.900-268A>G
XM_011510502.1:c.951-268A>G (EDAR)	XP_011508804.1:n.951-268A>G
XM_011510503.1:c.855-268A>G (EDAR)	XP_011508805.1:n.855-268A>G
XM_011510504.1:c.231-268A>G (EDAR)	XP_011508806.1:n.231-268A>G
XM_011510502.2:c.1044-268A>G (EDAR)	XP_011508804.2:n.1044-268A>G
XM_011510503.2:c.948-268A>G (EDAR)	XP_011508805.2:n.948-268A>G
XM_017004623.2:c.8370+135241T>C (RANBP2)	XP_016860112.1:n.8370+135241T>C
NM_022336.4:c.804-268A>G (EDAR) MANE Select	NP_071731.1:n.804-268A>G