Canonical Allele Identifier: CA439798360
Gene: ALB HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.74270056A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404339A>C , CM000666.2:g.73404339A>C GRCh38
NC_000004.11:g.74270056A>C , CM000666.1:g.74270056A>C GRCh37
NC_000004.10:g.74488920A>C NCBI36
NG_009291.1:g.5085A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.12A>C MANE Select ENSP00000295897.4:p.Val4=
ENST00000295897.8:c.12A>C ENSP00000295897.4:p.Val4=
ENST00000401494.7:c.12A>C ENSP00000384695.3:p.Val4=
ENST00000415165.6:c.12A>C ENSP00000401820.2:p.Val4=
ENST00000441319.5:c.48-30A>C ENSP00000392541.1:n.48-30A>C
ENST00000476441.6:c.12A>C ENSP00000423727.1:p.Val4=
ENST00000503124.5:c.-169A>C ENSP00000421027.1:n.-169A>C
ENST00000509063.5:c.12A>C ENSP00000422784.1:p.Val4=
ENST00000510166.5:n.53A>C
ENST00000514786.1:n.48+3A>C
ENST00000515133.5:n.53A>C
ENST00000621085.4:c.12A>C ENSP00000483421.1:p.Val4=
ENST00000621628.4:c.12A>C ENSP00000480485.1:p.Val4=
NM_000477.5:c.12A>C NP_000468.1:p.Val4=
NM_000477.6:c.12A>C NP_000468.1:p.Val4=
NM_000477.7:c.12A>C MANE Select NP_000468.1:p.Val4=