Canonical Allele Identifier: CA357234579

Gene: ALB

Linked Data

• dbSNP Id: rs1252055461
• gnomAD v2: 4-74270085-G-T
• MyVariant Identifiers: chr4:g.74270085G>T (hg19) ; chr4:g.73404368G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404368G>T , CM000666.2:g.73404368G>T	GRCh38
NC_000004.11:g.74270085G>T , CM000666.1:g.74270085G>T	GRCh37
NC_000004.10:g.74488949G>T	NCBI36
NG_009291.1:g.5114G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.41G>T MANE Select	ENSP00000295897.4:p.Ser14Ile
ENST00000295897.8:c.41G>T	ENSP00000295897.4:p.Ser14Ile
ENST00000401494.7:c.41G>T	ENSP00000384695.3:p.Ser14Ile
ENST00000415165.6:c.41G>T	ENSP00000401820.2:p.Ser14Ile
ENST00000441319.5:c.48-1G>T	ENSP00000392541.1:n.48-1G>T
ENST00000476441.6:c.41G>T	ENSP00000423727.1:p.Ser14Ile
ENST00000503124.5:c.-140G>T	ENSP00000421027.1:n.-140G>T
ENST00000509063.5:c.41G>T	ENSP00000422784.1:p.Ser14Ile
ENST00000510166.5:n.82G>T
ENST00000514786.1:n.48+32G>T
ENST00000515133.5:n.82G>T
ENST00000621085.4:c.41G>T	ENSP00000483421.1:p.Ser14Ile
ENST00000621628.4:c.41G>T	ENSP00000480485.1:p.Ser14Ile
NM_000477.5:c.41G>T	NP_000468.1:p.Ser14Ile
NM_000477.6:c.41G>T	NP_000468.1:p.Ser14Ile
NM_000477.7:c.41G>T MANE Select	NP_000468.1:p.Ser14Ile