Canonical Allele Identifier: CA439799551

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275195G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409478G>T , CM000666.2:g.73409478G>T	GRCh38
NC_000004.11:g.74275195G>T , CM000666.1:g.74275195G>T	GRCh37
NC_000004.10:g.74494059G>T	NCBI36
NG_009291.1:g.10224G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.606G>T MANE Select	ENSP00000295897.4:p.Leu202=
ENST00000295897.8:c.606G>T	ENSP00000295897.4:p.Leu202=
ENST00000401494.7:c.261G>T	ENSP00000384695.3:p.Leu87=
ENST00000415165.6:c.138-2518G>T	ENSP00000401820.2:n.138-2518G>T
ENST00000476441.6:c.203G>T	ENSP00000423727.1:p.Cys68Phe
ENST00000503124.5:c.156G>T	ENSP00000421027.1:p.Leu52=
ENST00000505649.5:n.292G>T
ENST00000509063.5:c.606G>T	ENSP00000422784.1:p.Leu202=
ENST00000511370.1:c.139G>T
ENST00000514786.1:n.575G>T
ENST00000621085.4:c.490+116G>T	ENSP00000483421.1:n.490+116G>T
ENST00000621628.4:c.486+402G>T	ENSP00000480485.1:n.486+402G>T
NM_000477.5:c.606G>T	NP_000468.1:p.Leu202=
NM_000477.6:c.606G>T	NP_000468.1:p.Leu202=
NM_000477.7:c.606G>T MANE Select	NP_000468.1:p.Leu202=