Canonical Allele Identifier: CA29824480

Gene: HJV

Linked Data

• ClinVar Variation Id: 1554796
• ClinVar RCV Id: RCV002199727
• dbSNP Id: rs1056084922
• MyVariant Identifiers: chr1:g.145415817C>G (hg19) ; chr1:g.146019196G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146019196G>C , CM000663.2:g.146019196G>C	GRCh38
NC_000001.10:g.145415817C>G , CM000663.1:g.145415817C>G	GRCh37
NC_000001.9:g.144127174C>G	NCBI36
NG_011568.1:g.7627C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336751.11:c.636C>G MANE Select	ENSP00000337014.5:p.Ala212=
ENST00000636675.1:c.-21-496C>G	ENSP00000490072.1:n.-21-496C>G
ENST00000336751.10:c.636C>G	ENSP00000337014.5:p.Ala212=
ENST00000357836.5:c.297C>G	ENSP00000350495.5:p.Ala99=
ENST00000475797.1:c.-21-496C>G	ENSP00000425716.1:n.-21-496C>G
ENST00000497365.5:c.-21-496C>G	ENSP00000421820.1:n.-21-496C>G
ENST00000634927.1:c.135-496C>G	ENSP00000489347.1:n.135-496C>G
NM_001316767.1:c.-21-496C>G	NP_001303696.1:n.-21-496C>G
NM_145277.4:c.297C>G	NP_660320.3:p.Ala99=
NM_202004.3:c.-21-496C>G	NP_973733.1:n.-21-496C>G
NM_213652.3:c.-21-496C>G	NP_998817.1:n.-21-496C>G
NM_213653.3:c.636C>G	NP_998818.1:p.Ala212=
XM_005272932.1:c.636C>G	XP_005272989.1:p.Ala212=
NM_001316767.2:c.-21-496C>G	NP_001303696.1:n.-21-496C>G
NM_145277.5:c.297C>G	NP_660320.3:p.Ala99=
NM_202004.4:c.-21-496C>G	NP_973733.1:n.-21-496C>G
NM_213652.4:c.-21-496C>G	NP_998817.1:n.-21-496C>G
NM_001379352.1:c.636C>G	NP_001366281.1:p.Ala212=
NM_213653.4:c.636C>G MANE Select	NP_998818.1:p.Ala212=