Canonical Allele Identifier: CA439798416

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74270110T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404393T>C , CM000666.2:g.73404393T>C	GRCh38
NC_000004.11:g.74270110T>C , CM000666.1:g.74270110T>C	GRCh37
NC_000004.10:g.74488974T>C	NCBI36
NG_009291.1:g.5139T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.66T>C MANE Select	ENSP00000295897.4:p.Phe22=
ENST00000295897.8:c.66T>C	ENSP00000295897.4:p.Phe22=
ENST00000401494.7:c.66T>C	ENSP00000384695.3:p.Phe22=
ENST00000415165.6:c.66T>C	ENSP00000401820.2:p.Phe22=
ENST00000441319.5:c.72T>C	ENSP00000392541.1:p.Phe24=
ENST00000476441.6:c.66T>C	ENSP00000423727.1:p.Phe22=
ENST00000503124.5:c.-115T>C	ENSP00000421027.1:n.-115T>C
ENST00000509063.5:c.66T>C	ENSP00000422784.1:p.Phe22=
ENST00000510166.5:n.107T>C
ENST00000514786.1:n.48+57T>C
ENST00000515133.5:n.107T>C
ENST00000621085.4:c.66T>C	ENSP00000483421.1:p.Phe22=
ENST00000621628.4:c.66T>C	ENSP00000480485.1:p.Phe22=
NM_000477.5:c.66T>C	NP_000468.1:p.Phe22=
NM_000477.6:c.66T>C	NP_000468.1:p.Phe22=
NM_000477.7:c.66T>C MANE Select	NP_000468.1:p.Phe22=