Canonical Allele Identifier: CA439800396

Gene: ALB

Linked Data

• gnomAD v4: 4-73415167-G-T
• MyVariant Identifiers: chr4:g.74280884G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415167G>T , CM000666.2:g.73415167G>T	GRCh38
NC_000004.11:g.74280884G>T , CM000666.1:g.74280884G>T	GRCh37
NC_000004.10:g.74499748G>T	NCBI36
NG_009291.1:g.15913G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1191G>T MANE Select	ENSP00000295897.4:p.Val397=
ENST00000295897.8:c.1191G>T	ENSP00000295897.4:p.Val397=
ENST00000401494.7:c.846G>T	ENSP00000384695.3:p.Val282=
ENST00000415165.6:c.615G>T	ENSP00000401820.2:p.Val205=
ENST00000476441.6:c.*470G>T	ENSP00000423727.1:n.*470G>T
ENST00000484992.1:n.511G>T
ENST00000503124.5:c.741G>T	ENSP00000421027.1:p.Val247=
ENST00000504043.1:n.194G>T
ENST00000505649.5:n.877G>T
ENST00000509063.5:c.1191G>T	ENSP00000422784.1:p.Val397=
ENST00000511370.1:c.724G>T
ENST00000621085.4:c.552G>T	ENSP00000483421.1:p.Val184=
ENST00000621628.4:c.552G>T	ENSP00000480485.1:p.Val184=
NM_000477.5:c.1191G>T	NP_000468.1:p.Val397=
NM_000477.6:c.1191G>T	NP_000468.1:p.Val397=
NM_000477.7:c.1191G>T MANE Select	NP_000468.1:p.Val397=