Canonical Allele Identifier: CA439948115

Gene: ALB

Linked Data

• gnomAD v4: 4-73413458-G-C
• MyVariant Identifiers: chr4:g.74279175G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413458G>C , CM000666.2:g.73413458G>C	GRCh38
NC_000004.11:g.74279175G>C , CM000666.1:g.74279175G>C	GRCh37
NC_000004.10:g.74498039G>C	NCBI36
NG_009291.1:g.14204G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.882G>C MANE Select	ENSP00000295897.4:p.Ser294=
ENST00000295897.8:c.882G>C	ENSP00000295897.4:p.Ser294=
ENST00000401494.7:c.537G>C	ENSP00000384695.3:p.Ser179=
ENST00000415165.6:c.306G>C	ENSP00000401820.2:p.Ser102=
ENST00000476441.6:c.*161G>C	ENSP00000423727.1:n.*161G>C
ENST00000484992.1:n.202G>C
ENST00000503124.5:c.432G>C	ENSP00000421027.1:p.Ser144=
ENST00000505649.5:n.568G>C
ENST00000509063.5:c.882G>C	ENSP00000422784.1:p.Ser294=
ENST00000511370.1:c.415G>C
ENST00000621085.4:c.491-1648G>C	ENSP00000483421.1:n.491-1648G>C
ENST00000621628.4:c.487-1644G>C	ENSP00000480485.1:n.487-1644G>C
NM_000477.5:c.882G>C	NP_000468.1:p.Ser294=
NM_000477.6:c.882G>C	NP_000468.1:p.Ser294=
NM_000477.7:c.882G>C MANE Select	NP_000468.1:p.Ser294=