Canonical Allele Identifier: CA420250410

Gene: HJV

Linked Data

• MyVariant Identifiers: chr1:g.145415899T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146019114A>G , CM000663.2:g.146019114A>G	GRCh38
NC_000001.10:g.145415899T>C , CM000663.1:g.145415899T>C	GRCh37
NC_000001.9:g.144127256T>C	NCBI36
NG_011568.1:g.7709T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336751.11:c.657+61T>C MANE Select	ENSP00000337014.5:n.657+61T>C
ENST00000636675.1:c.-21-414T>C	ENSP00000490072.1:n.-21-414T>C
ENST00000336751.10:c.657+61T>C	ENSP00000337014.5:n.657+61T>C
ENST00000357836.5:c.318+61T>C	ENSP00000350495.5:n.318+61T>C
ENST00000475797.1:c.-21-414T>C	ENSP00000425716.1:n.-21-414T>C
ENST00000497365.5:c.-21-414T>C	ENSP00000421820.1:n.-21-414T>C
ENST00000634927.1:c.135-414T>C	ENSP00000489347.1:n.135-414T>C
NM_001316767.1:c.-21-414T>C	NP_001303696.1:n.-21-414T>C
NM_145277.4:c.318+61T>C	NP_660320.3:n.318+61T>C
NM_202004.3:c.-21-414T>C	NP_973733.1:n.-21-414T>C
NM_213652.3:c.-21-414T>C	NP_998817.1:n.-21-414T>C
NM_213653.3:c.657+61T>C	NP_998818.1:n.657+61T>C
XM_005272932.1:c.657+61T>C	XP_005272989.1:n.657+61T>C
NM_001316767.2:c.-21-414T>C	NP_001303696.1:n.-21-414T>C
NM_145277.5:c.318+61T>C	NP_660320.3:n.318+61T>C
NM_202004.4:c.-21-414T>C	NP_973733.1:n.-21-414T>C
NM_213652.4:c.-21-414T>C	NP_998817.1:n.-21-414T>C
NM_001379352.1:c.657+61T>C	NP_001366281.1:n.657+61T>C
NM_213653.4:c.657+61T>C MANE Select	NP_998818.1:n.657+61T>C