Canonical Allele Identifier: CA439799222

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74274515T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408798T>C , CM000666.2:g.73408798T>C	GRCh38
NC_000004.11:g.74274515T>C , CM000666.1:g.74274515T>C	GRCh37
NC_000004.10:g.74493379T>C	NCBI36
NG_009291.1:g.9544T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.475T>C MANE Select	ENSP00000295897.4:p.Leu159=
ENST00000295897.8:c.475T>C	ENSP00000295897.4:p.Leu159=
ENST00000401494.7:c.138-557T>C	ENSP00000384695.3:n.138-557T>C
ENST00000415165.6:c.138-3198T>C	ENSP00000401820.2:n.138-3198T>C
ENST00000441319.5:c.481T>C	ENSP00000392541.1:p.Leu161=
ENST00000476441.6:c.80-557T>C	ENSP00000423727.1:n.80-557T>C
ENST00000503124.5:c.33-557T>C	ENSP00000421027.1:n.33-557T>C
ENST00000505649.5:n.161T>C
ENST00000509063.5:c.475T>C	ENSP00000422784.1:p.Leu159=
ENST00000510166.5:n.511T>C
ENST00000514786.1:n.444T>C
ENST00000515133.5:n.516T>C
ENST00000621085.4:c.475T>C	ENSP00000483421.1:p.Leu159=
ENST00000621628.4:c.475T>C	ENSP00000480485.1:p.Leu159=
NM_000477.5:c.475T>C	NP_000468.1:p.Leu159=
NM_000477.6:c.475T>C	NP_000468.1:p.Leu159=
NM_000477.7:c.475T>C MANE Select	NP_000468.1:p.Leu159=