Canonical Allele Identifier: CA99696385
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs146708617
COSMIC: COSM109114

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404330G>A , CM000666.2:g.73404330G>A GRCh38
NC_000004.11:g.74270047G>A , CM000666.1:g.74270047G>A GRCh37
NC_000004.10:g.74488911G>A NCBI36
NG_009291.1:g.5076G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.3G>A MANE Select ENSP00000295897.4:p.Met1Ile
ENST00000295897.8:c.3G>A ENSP00000295897.4:p.Met1Ile
ENST00000401494.7:c.3G>A ENSP00000384695.3:p.Met1Ile
ENST00000415165.6:c.3G>A ENSP00000401820.2:p.Met1Ile
ENST00000441319.5:n.48-39G>A ENSP00000392541.1:n.48-39G>A
ENST00000476441.6:c.3G>A ENSP00000423727.1:p.Met1Ile
ENST00000503124.5:c.-178G>A ENSP00000421027.1:n.-178G>A
ENST00000509063.5:c.3G>A ENSP00000422784.1:p.Met1Ile
ENST00000510166.5:n.44G>A
ENST00000514786.1:n.42G>A
ENST00000515133.5:n.44G>A
ENST00000621085.4:c.3G>A ENSP00000483421.1:p.Met1Ile
ENST00000621628.4:c.3G>A ENSP00000480485.1:p.Met1Ile
NM_000477.5:c.3G>A NP_000468.1:p.Met1Ile
NM_000477.6:c.3G>A NP_000468.1:p.Met1Ile
NM_000477.7:c.3G>A MANE Select NP_000468.1:p.Met1Ile