Canonical Allele Identifier: CA127904
Gene: ALB HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.73415162A>G
GRCh37 chr4:g.74280879A>G
Revel Score:
ENST00000295897 (MANE Select) 0.262
ENST00000415165 0.262
ENST00000329326 0.262
ENST00000503124 0.262
ENST00000509063 0.262
ENST00000401494 0.262
ENST00000430202 0.262
ENST00000511370 0.105
ClinVar RCV:
RCV000019844
ClinVar Variation:
18198
dbSNP:
78166690
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415162A>G , CM000666.2:g.73415162A>G GRCh38
NC_000004.11:g.74280879A>G , CM000666.1:g.74280879A>G GRCh37
NC_000004.10:g.74499743A>G NCBI36
NG_009291.1:g.15908A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.1186A>G MANE Select ENSP00000295897.4:p.Lys396Glu
ENST00000295897.8:c.1186A>G ENSP00000295897.4:p.Lys396Glu
ENST00000401494.7:c.841A>G ENSP00000384695.3:p.Lys281Glu
ENST00000415165.6:c.610A>G ENSP00000401820.2:p.Lys204Glu
ENST00000476441.6:c.*465A>G ENSP00000423727.1:n.*465A>G
ENST00000484992.1:n.506A>G
ENST00000503124.5:c.736A>G ENSP00000421027.1:p.Lys246Glu
ENST00000504043.1:n.189A>G
ENST00000505649.5:n.872A>G
ENST00000509063.5:c.1186A>G ENSP00000422784.1:p.Lys396Glu
ENST00000511370.1:c.719A>G
ENST00000621085.4:c.547A>G ENSP00000483421.1:p.Lys183Glu
ENST00000621628.4:c.547A>G ENSP00000480485.1:p.Lys183Glu
NM_000477.5:c.1186A>G NP_000468.1:p.Lys396Glu
NM_000477.6:c.1186A>G NP_000468.1:p.Lys396Glu
NM_000477.7:c.1186A>G MANE Select NP_000468.1:p.Lys396Glu
Search 100 bp 5'
Search 100 bp 3'